Category history - Genetics

From WikiLectures

Time Page Name Author of this revision Description Flags
2024-03-18 17:15 Allelic heterogeneity Nandini
2024-03-18 17:11 Alkaptonuria Nandini
2024-03-18 16:58 Additive model of polygenic inheritance Nandini
2024-02-14 17:36 Burton's agammaglobulinemia Bryce Seguin
2024-02-07 09:58 Chromosomal determination of sex Paraskevi Chatziloizou Added links
2024-02-05 15:45 Antigen Jakub Jan Kvašňák
2024-02-03 14:40 Cri du chat syndrome Jakub Jan Kvašňák
2024-02-03 14:40 Cri du chat syndrome Jakub Jan Kvašňák
2024-02-03 14:37 Cri du chat syndrome Jakub Jan Kvašňák
2024-02-03 14:31 Cri du chat syndrome Jakub Jan Kvašňák /* Used literature */
2024-02-03 14:28 Cri du chat syndrome Jakub Jan Kvašňák /* References */ added categories
2024-01-26 22:17 Cell cooperation in the B immune response Jakub Jan Kvašňák /* Links */ fixed category, translated citation
2024-01-23 14:04 Mitochondrial diseases / Respiratory chain enzyme deficiency Jakub Jan Kvašňák /* Used literature */
2024-01-23 14:04 Mitochondrial diseases / Respiratory chain enzyme deficiency Jakub Jan Kvašňák /* Used literature */
2024-01-23 14:01 Mitochondrial diseases / Respiratory chain enzyme deficiency Jakub Jan Kvašňák /* Used literature */
2024-01-23 14:01 Mitochondrial diseases / Respiratory chain enzyme deficiency Jakub Jan Kvašňák /* Used literature */
2024-01-23 14:00 Mitochondrial diseases / Respiratory chain enzyme deficiency Jakub Jan Kvašňák /* Used literature */
2024-01-23 14:00 Mitochondrial diseases / Respiratory chain enzyme deficiency Jakub Jan Kvašňák /* Used literature */
2024-01-23 13:58 Mitochondrial diseases / Respiratory chain enzyme deficiency Jakub Jan Kvašňák fixing and actually translating citations and categories
2024-01-23 13:41 Inhibitors (genetics) Jakub Jan Kvašňák /* References */ fixed citation
2024-01-22 16:35 Biological characteristics of tumors Tereza Filipová Editace a přidání kategorií.
2024-01-22 15:13 Control of gene expression and proteosynthesis in eukaryotes Jakub Jan Kvašňák /* Resources */ fixed category typo
2024-01-21 18:43 Autoimunitní lymfoproliferativní syndrom Tereza Filipová Editace a přidání kategorie.
2024-01-19 17:37 Apoptosis and clinical consequences of its dysregulation Cateducated added categories
2024-01-18 16:06 Amplification and expression of the isolated gene in the host cell Tereza Filipová Editace a přidání kategorií.
2024-01-18 12:02 Cowden's syndrome SatPet
2024-01-18 09:08 Alport's syndrome SatPet
2024-01-17 18:28 Li-Fraumeni syndrome Cateducated added category
2024-01-17 18:28 Meiosis, its regulation and disturbances Cateducated added category
2024-01-17 18:24 Mental retardation Cateducated added categories
2024-01-17 18:21 Metabolic osteopathies Cateducated added categories
2024-01-17 17:40 Allelic heterogeneity Tereza Filipová Přidání kategorie.
2024-01-16 21:58 Hemoglobinopathy Cateducated added categories
2024-01-16 21:39 DNA viruses Cateducated added category
2024-01-16 21:39 DNA fingerprinting Cateducated added category
2024-01-16 21:39 DNA (nucleic acid) Cateducated added category
2024-01-16 21:39 DNA Sequencing Cateducated added categories
2024-01-16 17:27 A sublethal gene Tereza Filipová Editace a přidání kategorie.
2024-01-15 20:47 Biochemistry of genetic engineering Cateducated added category
2024-01-15 20:43 Bacterial cell wall Cateducated added category
2024-01-15 20:40 Automatic analysis of 2D polyacrylamide gels in the diagnosis of DNA polymorphisms Cateducated added category
2024-01-15 20:39 Autophagy, Hayflick's limit, telomerase Cateducated added category
2024-01-15 20:38 Autosomally inherited agammaglobulinemia Cateducated added categories
2024-01-15 20:37 Autosome Cateducated added category
2024-01-15 20:28 Autoimmune lymphoproliferative syndrome Cateducated added categories
2024-01-15 15:16 DsDNA Cateducated added categories
2024-01-14 21:40 DiGeorge syndrome Cateducated added category
2024-01-14 21:39 DiGeorge syndrome Cateducated added categories
2024-01-14 21:39 DiGeorge syndrome Cateducated added categories
2024-01-14 21:38 DiGeorge syndrome Cateducated added categories
2024-01-14 17:27 Phenotype Michaela Rumlerová Přidání kategorií a editace
2024-01-14 17:19 Evolution Michaela Rumlerová Úprava kategorií a citací
2024-01-14 15:43 Malignant Michaela Rumlerová
2024-01-13 16:27 Prion Michaela Rumlerová Přidání kategorií
2024-01-10 19:39 Aging of the organism Beloslava Erofeeva added categories
2024-01-10 19:37 Additive model of polygenic inheritance Beloslava Erofeeva added categories
2024-01-10 19:04 Alkaptonuria Beloslava Erofeeva added categories
2024-01-10 18:58 Heredity (signpost) Jakub Jan Kvašňák translated category
2024-01-06 14:41 Autosomal dominant inheritance in pedigree and experiment, examples of traits in man
2024-01-06 14:39 Autosomal dominant inheritance in pedigree and experiment, examples of traits in man
2024-01-06 14:38 Autosomal dominant inheritance in pedigree and experiment, examples of traits in man
2024-01-03 17:26 A decision mechanism for the destruction of non-functional proteins
2024-01-03 17:24 A decision mechanism for the destruction of non-functional proteins edited
2024-01-01 21:10 PARK genes Jakub Jan Kvašňák /* References */ fixed category
2024-01-01 20:53 Structural chromosomal aberrations Jakub Jan Kvašňák /* Used literature */ fixing citations and categories
2024-01-01 20:52 Structural chromosomal aberrations Jakub Jan Kvašňák /* Related articles */
2024-01-01 20:52 Structural chromosomal aberrations Jakub Jan Kvašňák /* Cri du chat syndrome */
2024-01-01 20:51 Structural chromosomal aberrations Jakub Jan Kvašňák /* Examples of structural aberration */ fixing image and links
2023-12-24 08:17 Human karyotype, methods of its examination Viktorie Koberová me
2023-12-24 08:16 Human karyotype, methods of its examination Viktorie Koberová me
2023-12-24 08:15 Chromatin Viktorie Koberová me
2023-12-24 08:04 Hereditary immunodeficiencies Viktorie Koberová me
2023-12-23 08:11 Beckwith-Wiedemann Syndrome Viktorie Koberová me
2023-12-23 08:09 Angelman Syndrome Viktorie Koberová me
2023-12-23 08:08 Gametogenesis (Coursebook) Viktorie Koberová me
2023-12-23 08:06 Genetic linkage Viktorie Koberová me
2023-12-22 07:26 Dihybridism Viktorie Koberová me
2023-12-22 07:24 Genotype Variation, Mutations and Recombination Viktorie Koberová me
2023-12-22 07:18 Autosomal recessive inheritance in pedigree and experiment, examples of traits in man Viktorie Koberová me
2023-12-21 21:08 APC Resistence Avantika Subhash catergories
2023-12-21 21:06 Achondroplasia Avantika Subhash categories
2023-12-21 17:33 Congenital developmental defects Cateducated added categories
2023-12-21 17:32 Congenital developmental defects Cateducated /* Historie */
2023-12-21 17:31 Congenital developmental defects of the respiratory system Cateducated added categories
2023-12-21 17:29 Congenital glycosylation disorders Cateducated added categories
2023-12-21 17:26 Congenital steep talus Cateducated added categories
2023-12-21 17:24 Conjugation, transformation, transduction Cateducated added categories
2023-12-21 17:24 Conjugation, transformation, transduction Cateducated added categories
2023-12-19 21:22 Chromatin Jakub Jan Kvašňák /* Heterochromatin and Euchromatin */
2023-12-19 21:22 Chromatin Jakub Jan Kvašňák /* References */ fixing citations
2023-12-19 14:19 Osteogenesis imperfecta Viktorie Koberová me
2023-12-19 14:19 Osteogenesis imperfecta Viktorie Koberová me
2023-12-19 14:19 Osteogenesis imperfecta Viktorie Koberová me
2023-12-19 14:18 Osteogenesis imperfecta Viktorie Koberová me
2023-12-16 08:40 Bacterial cell wall Viktorie Koberová me
2023-12-16 08:38 Bacterial cell wall Viktorie Koberová me
2023-12-16 08:37 Bacterial cell wall Viktorie Koberová me
2023-12-15 14:27 Bacterial cell wall Viktorie Koberová me
2023-12-15 14:27 Bacterial cell wall Viktorie Koberová me
2023-12-15 14:27 Bacterial cell wall Viktorie Koberová me
2023-12-09 09:19 Cystic Fibrosis Viktorie Koberová add links and pictures me
2023-12-07 18:45 Mutagenesis Jakub Jan Kvašňák /* Resources */
2023-12-07 18:44 Mutagenesis Jakub Jan Kvašňák /* Resources */
2023-12-07 18:44 Mutagenesis Jakub Jan Kvašňák /* Resources */
2023-12-07 18:44 Mutagenesis Jakub Jan Kvašňák /* Resources */ fixing citations
2023-11-30 16:46 In vitro fertilization Jakub Jan Kvašňák /* Other methods related to IVF */
2023-11-30 16:46 In vitro fertilization Jakub Jan Kvašňák /* references */ fixing categories
2023-11-30 16:45 Genetic maps and their meaning Jakub Jan Kvašňák /* Links */ fixing categories
2023-11-30 16:45 Map of the human genome, HUGO, use Jakub Jan Kvašňák /* References */ fixing categories
2023-11-30 16:44 The genetic code Jakub Jan Kvašňák /* Links */ fixing categories
2023-11-30 16:44 Genetic modifications Jakub Jan Kvašňák /* References */ fixing categories
2023-11-30 16:44 Evolution and speciation at the molecular level Jakub Jan Kvašňák /* References */ fixing categories
2023-11-30 16:43 Gene Jakub Jan Kvašňák /* Related articles */ fixed links and categories
2023-11-30 16:42 Manifestations of developmental toxicity Jakub Jan Kvašňák /* References */ fixed categories
2023-11-30 11:43 Cell Gwenhwyfar Ania Gonnot Added links and categories
2023-11-29 12:04 Antigen Added categories
2023-11-29 12:01 AB0 system (English) Gwenhwyfar Ania Gonnot Added categories
2023-11-25 17:29 Achondroplasia Paraskevi Chatziloizou Remove nonexistent links
2023-11-24 21:20 Non-positional Leg Defects Jakub Jan Kvašňák
2023-11-24 21:18 Non-positional Leg Defects Jakub Jan Kvašňák /* References */
2023-11-24 21:18 Numerical chromosome abnormalities Jakub Jan Kvašňák /* References */
2023-11-24 21:17 Hyperimmunoglobulinemia IgM syndrome/other types Jakub Jan Kvašňák /* References */
2023-11-24 21:16 Hereditary metabolic disorders/Genetic background Jakub Jan Kvašňák /* Source */
2023-11-24 21:12 Nephronophthisis Jakub Jan Kvašňák /* Related articles */
2023-11-24 21:07 Congenital multiple exostoses Jakub Jan Kvašňák /* Refrences */
2023-11-24 21:07 Syndromes due to aneuploidy of gonosomes Jakub Jan Kvašňák /* Source */
2023-11-24 21:04 Congenital malformations of the respiratory system Jakub Jan Kvašňák /* Bibliography */
2023-11-24 21:02 Meningocele Jakub Jan Kvašňák /* Source */
2023-11-24 21:01 Meningocele Jakub Jan Kvašňák /* References */
2023-11-24 21:00 Meningocele Jakub Jan Kvašňák /* Source */
2023-11-24 20:58 Cowden's syndrome Mkvas1 /* External links */
2023-11-24 20:58 Cowden's syndrome Mkvas1 /* External links */
2023-11-24 20:57 Cowden's syndrome Mkvas1 /* External links */
2023-11-24 20:57 Cowden's syndrome Mkvas1 /* External links */
2023-11-24 20:48 Congenital diaphragmatic hernia Jakub Jan Kvašňák /* Literature */
2023-11-24 20:46 Developmental hip dysplasia Jakub Jan Kvašňák /* Use literature */
2023-11-24 20:46 Autosomal inherited agammaglobulinemia Jakub Jan Kvašňák /* Used literature */
2023-11-24 20:40 Multiple Congenital Exostoses Jakub Jan Kvašňák /* Refrences */
2023-11-24 20:36 Developmental disorders of the ear Jakub Jan Kvašňák /* References */
2023-11-24 20:36 Caring for a child with Down syndrome Jakub Jan Kvašňák /* References */
2023-11-24 20:36 Postnatal prevention of hereditary diseases Jakub Jan Kvašňák /* Source */
2023-11-24 20:29 Examination methods of inherited metabolic disorders Jakub Jan Kvašňák /* Indications leading to suspicion of IMD */
2023-11-24 20:28 Examination methods of inherited metabolic disorders Jakub Jan Kvašňák /* Diagnosis of IMD */
2023-11-24 20:27 Bloch-Sulzberg syndrome Jakub Jan Kvašňák /* References */
2023-11-24 20:23 Autoimunitní lymfoproliferativní syndrom Mkvas1
2023-11-24 20:22 Autoimunitní lymfoproliferativní syndrom Mkvas1
2023-11-24 20:21 Autoimunitní lymfoproliferativní syndrom Mkvas1
2023-11-24 20:18 Pes calcaneovalgus Jakub Jan Kvašňák /* References */
2023-11-24 20:12 Microdeletion syndromes Jakub Jan Kvašňák /* References */
2023-11-24 20:12 Prenatal screening of congenital anomalies Jakub Jan Kvašňák /* References */
2023-11-24 20:07 Chronic Granulomatous Disease Jakub Jan Kvašňák /* References */
2023-11-24 20:04 Metabolic osteopathy Jakub Jan Kvašňák
2023-11-24 20:04 Metabolic osteopathy Jakub Jan Kvašňák
2023-11-24 16:34 Congenital Heart Defects Jakub Jan Kvašňák /* Bibliography */
2023-11-24 16:33 Congenital Heart Defects Jakub Jan Kvašňák
2023-11-24 16:32 Congenital Heart Defects Jakub Jan Kvašňák
2023-11-24 16:30 Hereditary osteo-onychodysplasia Jakub Jan Kvašňák /* References */
2023-11-24 16:30 Congenital deformities of the auricle Jakub Jan Kvašňák /* Used literature */
2023-11-24 16:29 Peroxisomal leukodystrophy Jakub Jan Kvašňák /* Reference */
2023-11-24 16:29 Clubfoot (congenital talipes equinovarus) Jakub Jan Kvašňák /* External links */
2023-11-24 16:28 Clubfoot (congenital talipes equinovarus) Jakub Jan Kvašňák /* References */
2023-11-22 21:12 Aplasia radii congenita Jakub Jan Kvašňák /* References */
2023-11-22 21:12 Miller-Dieker syndrome Jakub Jan Kvašňák /* References */
2023-11-22 21:09 Examination methods in DMP Jakub Jan Kvašňák /* Indications leading to suspicion of DMP */
2023-11-22 21:09 Duchenn's muscular atrophy Jakub Jan Kvašňák /* Used literature */
2023-11-22 21:01 Congenital defects of the inner ear Jakub Jan Kvašňák /* References */
2023-11-22 21:00 Congenital adrenal hyperplasia Jakub Jan Kvašňák /* Reference */
2023-11-22 21:00 Congenital adrenal hyperplasia Jakub Jan Kvašňák /* Adrenogenital androgenic syndrome */
2023-11-22 21:00 Congenital adrenal hyperplasia Jakub Jan Kvašňák /* 21-hydroxylase deficiency */
2023-11-22 21:00 Congenital adrenal hyperplasia Jakub Jan Kvašňák /* 21-hydroxylase deficiency */
2023-11-22 20:59 Congenital adrenal hyperplasia Jakub Jan Kvašňák /* Adrenal disorders in children */
2023-11-22 20:57 Bartter syndrome Jakub Jan Kvašňák /* Clinical picture */
2023-11-22 20:57 Bartter syndrome Jakub Jan Kvašňák /* Clinical picture */
2023-11-22 20:56 Bartter syndrome Jakub Jan Kvašňák /* References */
2023-11-22 20:56 Bartter syndrome Jakub Jan Kvašňák /* References */
2023-11-22 20:55 Bartter syndrome Jakub Jan Kvašňák /* Pathogenesis */
2023-11-22 20:41 Marfan syndrome Jakub Jan Kvašňák /* Related articles */
2023-11-22 20:37 Hereditary disorders of sugar metabolism Jakub Jan Kvašňák /* References */
2023-11-22 20:34 Torticollis muscularis congenita Jakub Jan Kvašňák
2023-11-22 20:34 Prevention and early diagnosis of birth defects Jakub Jan Kvašňák /* References */
2023-11-22 20:33 Prevention and early diagnosis of birth defects Jakub Jan Kvašňák
2023-11-22 20:21 Amniocentesis Jakub Jan Kvašňák /* Used literature */
2023-11-22 20:21 Fragile X syndrome Jakub Jan Kvašňák /* References */
2023-11-22 20:17 Fabry Disease Jakub Jan Kvašňák /* Source */
2023-11-22 20:07 Marfan syndrome Jakub Jan Kvašňák /* References */
2023-11-19 20:47 Dog equinovarus congenitus Jakub Jan Kvašňák /* External links */
2023-11-19 11:18 Congenita muscularis torticollis Jakub Jan Kvašňák /* References */
2023-11-19 11:16 Primary immunodeficiency Jakub Jan Kvašňák /* Immunodeficiency caused by phagocytosis disorders */
2023-11-19 11:16 Primary immunodeficiency Jakub Jan Kvašňák /* References */
2023-11-19 11:15 Primary immunodeficiency Jakub Jan Kvašňák /* Source */
2023-11-19 11:14 Primary ciliary dyskinesia Jakub Jan Kvašňák /* Links */
2023-11-19 11:07 Primary immunodeficiencies Jakub Jan Kvašňák /* Used literature */
2023-11-17 18:26 A palindrome Jakub Jan Kvašňák /* References */
2023-11-17 10:51 X chromosome Jakub Jan Kvašňák
2023-11-15 19:34 Biology and genetics of viruses, importance in medicine Gwenhwyfar Ania Gonnot added links
2023-11-13 19:55 Thanatophoric dwarfism Jakub Jan Kvašňák /* Refrences */
2023-11-13 19:51 Positional defects of the leg Jakub Jan Kvašňák /* References */
2023-11-13 19:48 Severe congenital Kostmann neutropenia Jakub Jan Kvašňák /* Used literature */
2023-11-12 21:43 Promoter Jakub Jan Kvašňák
2023-11-12 21:37 Benign Jakub Jan Kvašňák
2023-11-12 09:28 Fragile X syndrome Sarah Muller
2023-11-12 09:27 Fragile X syndrome Sarah Muller
2023-11-11 23:23 Prenatal diagnosis Jakub Jan Kvašňák /* External links */
2023-11-11 17:27 Dysostosis cleidocranialis Laura Tašková
2023-11-11 17:21 Dysostosis cleidocranialis Laura Tašková deleted infobox, didnt work properly
2023-11-11 17:20 Dysostosis cleidocranialis Laura Tašková
2023-11-11 17:19 Dysostosis cleidocranialis Laura Tašková
2023-11-11 17:17 Dysostosis cleidocranialis Laura Tašková
2023-11-11 17:17 Dysostosis cleidocranialis Laura Tašková
2023-11-11 17:16 Dysostosis cleidocranialis Laura Tašková
2023-11-11 17:16 Dysostosis cleidocranialis Laura Tašková
2023-11-11 17:14 Dysostosis cleidocranialis Laura Tašková
2023-11-11 17:14 Dysostosis cleidocranialis Laura Tašková
2023-11-11 17:13 Dysostosis cleidocranialis Laura Tašková
2023-11-11 17:11 Dysostosis cleidocranialis Laura Tašková
2023-11-11 17:10 Dysostosis cleidocranialis Laura Tašková added infobox
2023-11-11 17:05 Dysostosis cleidocranialis Laura Tašková
2023-11-11 17:04 Dysostosis cleidocranialis Laura Tašková
2023-11-11 17:02 Dysostosis cleidocranialis Laura Tašková
2023-11-11 16:53 Dysostosis cleidocranialis Laura Tašková links to correct articles
2023-11-10 18:55 Charcot-Marie-Tooth Syndrome Jakub Jan Kvašňák /* References */
2023-11-10 18:46 Ectodermal dysplasia Jakub Jan Kvašňák /* Used literature */
2023-11-10 18:36 Williams-Beuren syndrome Jakub Jan Kvašňák /* Sources */
2023-11-10 18:30 Enchondromatosis Jakub Jan Kvašňák /* Related articles */
2023-11-10 18:30 Enchondromatosis Jakub Jan Kvašňák /* Related articles */
2023-11-10 18:21 Cherry stain Jakub Jan Kvašňák /* Related articles */
2023-11-10 11:37 Principles of therapy of hereditary diseases Jakub Jan Kvašňák /* Source */
2023-11-10 11:30 Crigler-Najjar syndrome Jakub Jan Kvašňák /* Source */
2023-11-10 11:30 Zellweger syndrome Jakub Jan Kvašňák /* References */
2023-11-10 11:29 Wilson's disease Jakub Jan Kvašňák
2023-11-10 11:29 Wilson's disease Jakub Jan Kvašňák /* Použitá literatura */
2023-11-10 11:28 Wilson's disease Jakub Jan Kvašňák /* Doporučená literatura */
2023-11-10 11:13 Severe Combined Immunodeficiency Disease Jakub Jan Kvašňák /* References */
2023-11-10 11:11 Position dog varus Jakub Jan Kvašňák /* References */
2023-11-10 11:11 Position dog varus Jakub Jan Kvašňák /* References */
2023-11-10 11:11 Position dog varus Jakub Jan Kvašňák /* References */
2023-11-10 11:11 Poland's anomaly Jakub Jan Kvašňák /* References */
2023-11-10 11:10 Urea cycle disorders Jakub Jan Kvašňák
2023-11-10 11:08 Urea cycle disorders Jakub Jan Kvašňák /* Prognosis */
2023-11-10 11:07 Duane Retraction Syndrome Jakub Jan Kvašňák /* Source */
2023-11-10 11:01 DeLange syndrome Jakub Jan Kvašňák /* References */
2023-11-10 11:00 Congenital malformations of the auricle Jakub Jan Kvašňák /* References */
2023-11-09 22:12 Rett syndrome Jakub Jan Kvašňák
2023-11-09 22:11 Rett syndrome Jakub Jan Kvašňák /* References */
2023-11-09 22:08 Fetus Jakub Jan Kvašňák /* Related articles */
2023-11-09 22:07 Fetus Jakub Jan Kvašňák /* Links */
2023-11-09 21:55 Urea Cycle Disorders Jakub Jan Kvašňák /* Reference */
2023-11-09 21:50 Wolf-Hirschhorn syndrome Jakub Jan Kvašňák /* References */
2023-11-08 20:40 Leukodystrophy Jakub Jan Kvašňák /* References */
2023-11-08 20:36 Metatarsus varus Jakub Jan Kvašňák /* Related articles */
2023-11-08 20:35 Hemoglobinopathies Jakub Jan Kvašňák /* Source */
2023-11-08 20:26 Hemochromatosis Jakub Jan Kvašňák
2023-11-01 20:52 Cystic fibrosis Jakub Jan Kvašňák /* External */
2023-11-01 20:27 Zellweger syndrome Jakub Jan Kvašňák /* References */
2023-10-29 20:35 47, XXX syndrome Jakub Jan Kvašňák
2023-10-29 20:35 47, XXX syndrome Jakub Jan Kvašňák
2023-10-29 20:35 47, XXX syndrome Jakub Jan Kvašňák
2023-10-02 19:56 Alport's syndrome Ahmed Bahaa Chaban
2023-10-02 19:48 Von Willebrand disease Ahmed Bahaa Chaban
2023-10-02 18:28 Hemoglobinopathies Ahmed Bahaa Chaban
2023-10-02 18:26 Hemochromatosis Ahmed Bahaa Chaban
2023-10-02 18:24 Sickle Cell Anemia Ahmed Bahaa Chaban
2023-10-02 18:09 Hemoglobinopathies Ahmed Bahaa Chaban
2023-10-02 18:08 Hemoglobinopathies Ahmed Bahaa Chaban
2023-10-02 18:07 Sickle Cell Anemia Ahmed Bahaa Chaban
2023-07-12 09:04 Severe congenital Kostmann neutropenia Andrea Rashovska references and categories corrected
2023-07-12 08:45 Congenita muscularis torticollis Andrea Rashovska References and categories corrected
2023-06-14 16:03 Hemochromatosis Egon Lenner
2023-06-14 15:58 Hemoglobinopathies Egon Lenner
2023-06-06 20:44 Metabolic osteopathy Hakam added citation
2023-06-02 15:05 Pes calcaneovalgus Michael Hartig Hartigm moved page [[Dog calcaneovalgus]] to [[Pes calcaneovalgus]] over redirect me
2023-06-02 15:04 Pes calcaneovalgus Michael Hartig Undo revision 86785 by [[Special:Contributions/Roshneekesh|Roshneekesh]] ([[User talk:Roshneekesh|talk]])
2023-06-01 03:09 Nuclear envelope Kimia Soltani fixed refrences
2023-05-31 15:47 Colorectal cancer Tereza Prokšíková
2023-05-31 15:47 Colorectal cancer Tereza Prokšíková
2023-05-31 15:46 Colorectal cancer Tereza Prokšíková
2023-05-31 15:45 Colorectal cancer Tereza Prokšíková
2023-05-31 15:41 Colorectal cancer Tereza Prokšíková
2023-05-31 15:10 Colorectal cancer Tereza Prokšíková
2023-05-31 15:05 Colorectal cancer Tereza Prokšíková
2023-05-31 14:56 Colorectal cancer Tereza Prokšíková
2023-05-31 14:40 Colorectal cancer Tereza Prokšíková
2023-05-31 14:38 Colorectal cancer Tereza Prokšíková
2023-05-31 14:35 Colorectal cancer Tereza Prokšíková
2023-05-31 14:34 Colorectal cancer Tereza Prokšíková
2023-05-31 14:31 Colorectal cancer Tereza Prokšíková
2023-05-31 14:25 Colorectal cancer Tereza Prokšíková me
2023-05-31 14:23 Colorectal cancer Tereza Prokšíková
2023-05-31 14:18 Colorectal cancer Tereza Prokšíková
2023-05-31 14:16 Colorectal cancer Tereza Prokšíková
2023-05-31 14:14 Colorectal cancer Tereza Prokšíková me
2023-05-31 14:13 Colorectal cancer Tereza Prokšíková
2023-05-31 14:03 Colorectal cancer Tereza Prokšíková
2023-05-31 14:01 Colorectal cancer Tereza Prokšíková
2023-05-31 13:33 Colorectal cancer Tereza Prokšíková
2023-05-31 13:28 Colorectal cancer Tereza Prokšíková
2023-05-31 13:24 Colorectal cancer Tereza Prokšíková
2023-05-31 13:14 Colorectal cancer Tereza Prokšíková
2023-05-31 12:47 Colorectal cancer Tereza Prokšíková
2023-05-31 12:44 Colorectal cancer Tereza Prokšíková
2023-05-30 17:27 Nuclear envelope Kimia Soltani fixed links,fixed refrences, fixed sentences
2023-05-30 16:03 Pes calcaneovalgus Roshnee Kesh Original text was from WikiSkripta (https://www.wikiskripta.eu/w/Pes_calcaneovalgus)
2023-05-30 16:01 Pes calcaneovalgus Roshnee Kesh Roshneekesh moved page [[Pes calcaneovalgus]] to [[Dog calcaneovalgus]]: Name change me
2023-05-30 13:04 Colorectal cancer Tereza Prokšíková
2023-05-28 22:11 Turner's Syndrome Warisha Amir /* MKN-10 classification */
2023-05-28 22:10 Turner's Syndrome Warisha Amir Original test is from: https://www.wikiskripta.eu/w/Turner%C5%AFv_syndrom
2023-05-28 22:10 Turner's Syndrome Warisha Amir
2023-05-28 22:06 Turner's Syndrome Warisha Amir
2023-05-28 22:04 Turner's Syndrome Warisha Amir
2023-05-28 22:03 Turner's Syndrome Warisha Amir
2023-05-28 22:02 Turner's Syndrome Warisha Amir
2023-05-28 22:01 Turner's Syndrome Warisha Amir
2023-05-28 21:58 Turner's Syndrome Warisha Amir
2023-05-28 21:57 Turner's Syndrome Warisha Amir
2023-05-28 21:55 Turner's Syndrome Warisha Amir Original test is from: https://www.wikiskripta.eu/w/Turner%C5%AFv_syndrom
2023-05-28 21:44 Turner's Syndrome Warisha Amir Original test is from: https://www.wikiskripta.eu/w/Turner%C5%AFv_syndrom
2023-05-28 21:41 Turner's Syndrome Warisha Amir Original test is from: https://www.wikiskripta.eu/w/Turner%C5%AFv_syndrom
2023-05-24 19:01 Screening of congenital developmental defects Matyáš Vláčil Checked by editor
2023-05-23 15:42 Mutation Sofia Filonova References and citation corrected, images corrected
2023-05-21 09:55 Niemann-Pick disease Sofia Filonova Text formatting
2023-05-21 09:41 Niemann-Pick disease Sofia Filonova Categories added, citations and the image corrected
2023-05-17 19:05 Niemann-Pick disease shaan ikrami
2023-05-15 19:07 Gene expression Jakub Jan Kvašňák
2023-05-15 19:07 Gene expression Jakub Jan Kvašňák
2023-05-15 19:04 Gardner's syndrome Jakub Jan Kvašňák
2023-05-15 18:53 Duplication Jakub Jan Kvašňák
2023-05-15 18:37 Clastogens Jakub Jan Kvašňák
2023-05-15 18:37 Congenital strain Jakub Jan Kvašňák
2023-05-15 18:29 Genomic DNA Jakub Jan Kvašňák
2023-05-15 18:08 Eugenics Jakub Jan Kvašňák
2023-05-15 18:07 The gene pool Jakub Jan Kvašňák
2023-05-15 17:55 Intercross Jakub Jan Kvašňák
2023-05-15 17:53 Fechtner-Epstein syndrome Jakub Jan Kvašňák
2023-05-13 17:34 Hyperimmunoglobulinemia IgM syndrome/other types emad alsaeedi
2023-05-13 17:32 Hyperimmunoglobulinemia IgM syndrome/other types emad alsaeedi
2023-05-13 17:11 Hyperimmunoglobulinemia IgM syndrome/other types emad alsaeedi
2023-05-10 08:14 Genetics of intelligence Jakub Jan Kvašňák
2023-05-10 08:14 Genetics of intelligence Jakub Jan Kvašňák
2023-05-01 08:54 Leukodystrophy Anna Fähnrichová me
2023-04-30 09:51 Apoptosis signaling disorders in tumor cells Sofia Filonova Internal links added, text formatting
2023-04-29 18:37 Hyperimmunoglobulinemia IgM syndrome/other types emad alsaeedi original text from Wikiskripta: Syndrom hyperimunoglobulinemie IgM/další typyhttps://www.wikiskripta.eu/index.php?curid=4130
2023-04-28 18:15 Apoptosis signaling disorders in tumor cells Sofia Filonova Citation corrected, categories added
2023-04-28 15:39 Colorectal cancer Tereza Prokšíková
2023-04-28 15:37 Colorectal cancer Tereza Prokšíková
2023-04-28 15:34 Colorectal cancer Tereza Prokšíková
2023-04-28 15:31 Colorectal cancer Tereza Prokšíková
2023-04-27 20:27 Severe congenital Kostmann neutropenia Tali
2023-04-27 20:21 Severe congenital Kostmann neutropenia Tali Tali Zerckes- article in translation process
2023-04-27 19:52 Congenita muscularis torticollis Tali
2023-04-27 19:34 Congenita muscularis torticollis Tali Tali Zerckes- article in translation process
2023-04-21 18:42 Apoptosis Matyáš Vláčil
2023-04-19 11:22 Apoptosis Andrea Rashovska Andyra moved page [[Apoptosis repetition]] to [[Apoptosis]]: corrrection me
2023-04-18 17:39 Apoptosis and Necrosis Matyáš Vláčil Matt moved page [[Apoptosis]] to [[Apoptosis and Necrosis]]: More fitting name me
2023-04-18 17:36 Apoptosis Matyáš Vláčil Checked by editor
2023-04-18 16:41 APC resistance Matyáš Vláčil Checked by editor
2023-04-17 20:04 Syndromes due to aneuploidy of autosomes Sofia Filonova Image added, minor visual edits, category corrected
2023-04-17 17:41 Syndromes due to aneuploidy of gonosomes Tereza Bergendyová
2023-04-17 17:41 Syndromes due to aneuploidy of gonosomes Tereza Bergendyová checked by the editor
2023-04-17 17:34 Syndromes due to aneuploidy of autosomes Tereza Bergendyová
2023-04-17 17:32 Syndromes due to aneuploidy of autosomes Tereza Bergendyová checked by the editor
2023-04-17 17:31 Syndromes due to aneuploidy of autosomes Tereza Bergendyová checked by the editor
2023-04-17 17:14 Syndrome 47, XXY Tereza Bergendyová checked by the editor
2023-04-17 17:09 Syndrome 47,XXX Tereza Bergendyová checked by the editor
2023-04-15 21:49 Fragile X syndrome
2023-04-15 21:49 Fragile X syndrome
2023-04-15 21:47 Fragile X syndrome Advay Arora
2023-04-15 21:45 Fragile X syndrome Advay Arora Created page with "<!---------------------------------------------------------------------------------------------------------------- * VLOŽENÝ ČLÁNEK * Pozor – tento článek je využí..."
2023-04-15 09:03 Apert syndrome Sofia Filonova Category is corrected, small editions in citation template, small visual editions (image size, notoc) me
2023-04-14 17:57 Srostlice (obstetrics) Veronika Kousalová
2023-04-14 17:56 Srostlice (obstetrics) Veronika Kousalová Original text from (https://www.wikiskripta.eu/index.php?curid=25248)
2023-04-14 17:45 Syndrome 47, XXY Created page with "[[File:I.png|thumb|Karyotype of 47,XYY syndrome]] '''The 47,XYY syndrome''' is caused by the presence of two or more [[wikiskripta:Chromozom_Y|Y chromosomes]] in the karyo..."
2023-04-14 17:36 Syndrome 47,XXX everything
2023-04-14 14:45 Collection of chorionic villi RRV8
2023-04-14 14:44 Collection of chorionic villi RRV8
2023-04-14 14:39 Collection of chorionic villi RRV8
2023-04-14 14:35 Collection of chorionic villi RRV8
2023-04-14 14:31 Collection of chorionic villi RRV8 Created page with "<noinclude>{{Checked | 20190307111556 | [[File:Antonín Šípek.jpg | 30px | link=User:Azrael]] [[User:Azrael|MUDr. Antonín Šípek]] -- WikiSkript:Organization|editing Wik..."
2023-04-13 19:25 Screening of congenital developmental defects Eliška Radová
2023-04-13 19:25 Screening of congenital developmental defects Eliška Radová
2023-04-13 19:21 Screening of congenital developmental defects Eliška Radová
2023-04-13 19:17 Screening of congenital developmental defects Eliška Radová
2023-04-13 18:26 Syndromes due to aneuploidy of gonosomes Michalis Papakyriacou Created page with " '''Aneuploidy''' = loss (monosomy) or presence of 1 or more [[chromosomes]] in the [[genome]] of a cell. * Causes: division disorder ( '''nondisjunction''' ) of homologous..."
2023-04-13 16:39 Syndromes due to aneuploidy of autosomes Created page with " Aneuploidy refers to the loss (monosomy) or presence of (one or more) chromosomes in the [[genome]] of a cell. '''The cause''' may be a division disorder (nondisjunction) of..."
2023-04-13 11:20 Screening of congenital developmental defects Eliška Radová
2023-04-13 10:54 Screening of congenital developmental defects Eliška Radová
2023-04-13 10:44 Screening of congenital developmental defects Eliška Radová
2023-04-13 10:04 Screening of congenital developmental defects Eliška Radová
2023-04-13 10:02 Screening of congenital developmental defects Eliška Radová
2023-04-13 09:58 Screening of congenital developmental defects Eliška Radová
2023-04-13 09:36 Screening of congenital developmental defects Eliška Radová Original text from WikiSkripta: Screening vrozených vývojových vad: https://www.wikiskripta.eu/index.php?curid=3341
2023-04-11 14:38 Chromosomal instability syndromes Michael Hartig Checked by editor
2023-04-11 14:36 Chromosomal instability syndromes Michael Hartig /* Recommended literature */
2023-04-11 14:36 Chromosomal instability syndromes Michael Hartig
2023-04-11 14:36 Chromosomal instability syndromes Michael Hartig me
2023-04-11 06:33 Leukodystrophy Erdi Beqiri Original text is from WikiSkripta: https://www.wikiskripta.eu/index.php?curid=22174
2023-04-11 06:32 Leukodystrophy Erdi Beqiri
2023-04-11 06:31 Leukodystrophy Fixed the links
2023-04-10 08:04 Screening of congenital developmental defects Eliška Radová
2023-04-10 07:55 Screening of congenital developmental defects Eliška Radová
2023-04-09 18:54 Congenital disorders of glycosylation Matyáš Vláčil Checked by editor.
2023-04-09 07:02 Wilms' tumor Sofia Filonova me
2023-04-09 06:58 Wilms' tumor Sofia Filonova internal links and category added
2023-04-09 06:53 Wilms' tumor Sofia Filonova citation and references corrected
2023-04-08 08:42 Screening of congenital developmental defects Eliška Radová
2023-04-08 08:38 Screening of congenital developmental defects Eliška Radová Original text from WikiSkripta: Screening vrozených vývojových vad: https://www.wikiskripta.eu/index.php?curid=3341
2023-04-08 08:08 Screening of congenital developmental defects Eliška Radová Blanked the page
2023-04-08 07:48 Screening of congenital developmental defects Eliška Radová Original text is from WikiSkripta: Screening vrozených vývojových vad: https://www.wikiskripta.eu/index.php?curid=3341
2023-04-04 18:32 Gonosomal recessive inheritance Sofia Filonova checked by editor
2023-04-02 18:50 Gonosomal recessive inheritance Jowel Jbara
2023-04-02 11:53 Fabry Disease Veronika Kousalová
2023-04-02 07:30 Gonosomal dominant inheritance Sofia Filonova checked by editor me
2023-04-01 19:26 Ehlers–Danlos syndrome Veronika Kousalová
2023-04-01 17:39 Gonosomal dominant inheritance Jowel Jbara
2023-04-01 17:39 Gonosomal dominant inheritance Jowel Jbara
2023-04-01 12:23 Chronic Granulomatous Disease Tereza Bergendyová checked by the editor
2023-03-31 17:01 Metabolic osteopathy Hakam
2023-03-31 17:00 Metabolic osteopathy Hakam Original Text from WikiScripta (https://www.wikiskripta.eu/index.php?curid=31312)
2023-03-31 15:27 Chronic Granulomatous Disease Ahmed Bahaa Chaban
2023-03-31 15:26 Chronic Granulomatous Disease Ahmed Bahaa Chaban
2023-03-31 15:22 Chronic Granulomatous Disease Ahmed Bahaa Chaban
2023-03-31 15:17 Chronic Granulomatous Disease Ahmed Bahaa Chaban
2023-03-31 14:27 Hemoglobinopathies Tereza Bergendyová
2023-03-31 14:25 Hemophilia Tereza Bergendyová
2023-03-31 13:53 Hemoglobinopathies Tereza Bergendyová
2023-03-31 13:52 Hemoglobinopathies Tereza Bergendyová checked by the editor
2023-03-31 13:45 Hemophilia Tereza Bergendyová
2023-03-31 13:45 Hemophilia Tereza Bergendyová checked by the editor
2023-03-30 13:52 Fabry Disease Tereza Bergendyová me
2023-03-30 13:50 Fabry Disease Tereza Bergendyová checked by the editor
2023-03-29 13:05 Hemoglobinopathies Jakub Jan Kvašňák /* Source */
2023-03-29 13:04 Hemoglobinopathies Jakub Jan Kvašňák /* Source */
2023-03-29 13:04 Hemoglobinopathies Jakub Jan Kvašňák /* Source */
2023-03-29 13:03 Hemoglobinopathies Jakub Jan Kvašňák
2023-03-28 18:56 Hemoglobinopathies Kiana Sadehmeymandi
2023-03-28 18:51 Hemoglobinopathies Kiana Sadehmeymandi
2023-03-28 18:50 Hemoglobinopathies Kiana Sadehmeymandi
2023-03-28 18:43 Hemoglobinopathies Kiana Sadehmeymandi
2023-03-28 18:35 Hemophilia Kiana Sadehmeymandi
2023-03-28 18:34 Hemophilia Kiana Sadehmeymandi
2023-03-28 18:34 Hemophilia Kiana Sadehmeymandi
2023-03-28 15:18 Hemophilia Kiana Sadehmeymandi
2023-03-28 15:13 Hemophilia Jakub Jan Kvašňák
2023-03-28 15:11 Hemophilia Jakub Jan Kvašňák
2023-03-28 15:11 Hemophilia Jakub Jan Kvašňák
2023-03-28 15:11 Hemophilia Jakub Jan Kvašňák
2023-03-28 13:26 Fabry Disease Veronika Kousalová
2023-03-27 21:46 Fabry Disease Veronika Kousalová
2023-03-27 21:44 Fabry Disease Veronika Kousalová
2023-03-27 21:43 Fabry Disease Veronika Kousalová
2023-03-27 21:43 Fabry Disease Veronika Kousalová
2023-03-27 21:42 Fabry Disease Veronika Kousalová Original text from (https://www.wikiskripta.eu/index.php?curid=69060)
2023-03-27 21:41 Fabry Disease Veronika Kousalová
2023-03-27 21:39 Fabry Disease Veronika Kousalová
2023-03-27 21:39 Fabry Disease Veronika Kousalová Original text from (https://www.wikiskripta.eu/index.php?curid=69060)
2023-03-27 21:36 Fabry Disease Veronika Kousalová
2023-03-27 21:34 Fabry Disease Veronika Kousalová Original text from (https://www.wikiskripta.eu/index.php?curid=69060)
2023-03-27 21:34 Fabry Disease Veronika Kousalová
2023-03-27 21:33 Fabry Disease Veronika Kousalová
2023-03-27 21:31 Fabry Disease Veronika Kousalová
2023-03-27 21:30 Fabry Disease Veronika Kousalová
2023-03-27 21:23 Fabry Disease Veronika Kousalová Original text from (https://www.wikiskripta.eu/index.php?curid=69060)
2023-03-27 21:22 Fabry Disease Veronika Kousalová Original text from (https://www.wikiskripta.eu/index.php?curid=69060)
2023-03-27 21:18 Fabry Disease Veronika Kousalová Original text from (https://www.wikiskripta.eu/index.php?curid=69060)
2023-03-27 21:09 Fabry Disease Veronika Kousalová Original text from (https://www.wikiskripta.eu/index.php?curid=69060)
2023-03-27 20:58 Fabry Disease Veronika Kousalová Original text from (https://www.wikiskripta.eu/index.php?curid=69060)
2023-03-27 20:56 Fabry Disease Veronika Kousalová Original text from (https://www.wikiskripta.eu/index.php?curid=69060)
2023-03-27 20:55 Fabry Disease Veronika Kousalová Original text from (https://www.wikiskripta.eu/index.php?curid=69060)
2023-03-27 20:53 Fabry Disease Veronika Kousalová Original text from (https://www.wikiskripta.eu/index.php?curid=69060)
2023-03-27 20:51 Fabry Disease Veronika Kousalová Original text from (https://www.wikiskripta.eu/index.php?curid=69060)
2023-03-27 20:47 Fabry Disease Veronika Kousalová Original text from (https://www.wikiskripta.eu/index.php?curid=69060)
2023-03-27 20:46 Fabry Disease Veronika Kousalová Original text from (https://www.wikiskripta.eu/index.php?curid=69060)
2023-03-27 20:45 Fabry Disease Veronika Kousalová Original text from (https://www.wikiskripta.eu/index.php?curid=69060)
2023-03-27 20:33 Fabry Disease Veronika Kousalová Original text from (https://www.wikiskripta.eu/index.php?curid=69060)
2023-03-27 20:28 Fabry Disease Original text from (https://www.wikiskripta.eu/index.php?curid=53542)
2023-03-27 20:01 Fabry Disease Veronika Kousalová
2023-03-27 20:00 Fabry Disease Veronika Kousalová Created page with "'''Fabry disease''' or '''sphingolipidosis''' is characterized as a metabolic [[Lysosomes|lysosomal]] disease with a frequency of 1:40,000. It is a gene mutation on the long a..."
2023-03-27 14:40 Sarcomeric and Non-sarcomeric forms of hypertrophic cardiomyopathy Jakub Jan Kvašňák /* Links */
2023-03-27 14:40 Sarcomeric and Non-sarcomeric forms of hypertrophic cardiomyopathy Jakub Jan Kvašňák /* References */
2023-03-27 14:39 Sarcomeric and Non-sarcomeric forms of hypertrophic cardiomyopathy Jakub Jan Kvašňák /* References */
2023-03-26 09:56 Congenital defects of the external and middle ear Anna Fähnrichová me
2023-03-25 16:16 Hemoglobinopathies Kiana Sadehmeymandi
2023-03-25 16:15 Hemoglobinopathies Kiana Sadehmeymandi
2023-03-25 16:02 Hemophilia Kiana Sadehmeymandi
2023-03-25 09:51 Huntington's disease Filip Kočka added categories
2023-03-24 11:10 Congenital defects of the external and middle ear Erdi Beqiri me
2023-03-24 11:08 Congenital defects of the external and middle ear Erdi Beqiri me
2023-03-24 11:07 Congenital defects of the external and middle ear Erdi Beqiri me
2023-03-24 11:07 Congenital defects of the external and middle ear Erdi Beqiri me
2023-03-24 11:06 Congenital defects of the external and middle ear Erdi Beqiri me
2023-03-24 11:06 Congenital defects of the external and middle ear Erdi Beqiri me
2023-03-24 11:05 Congenital defects of the external and middle ear Erdi Beqiri me
2023-03-24 10:58 Congenital defects of the external and middle ear Erdi Beqiri me
2023-03-24 10:58 Congenital defects of the external and middle ear Erdi Beqiri me
2023-03-24 10:55 Congenital defects of the external and middle ear Erdi Beqiri me
2023-03-24 10:47 Congenital defects of the external and middle ear Erdi Beqiri Translated the article
2023-03-23 01:08 Evolution of the species Homo sapiens /* Australopithecus */
2023-03-23 01:07 Evolution of the species Homo sapiens /* Australopithecus */
2023-03-22 15:25 Restriction fragment length polymorphism Sofia Filonova checked by editor me
2023-03-21 19:20 Gonosomal dominant inheritance Jowel Jbara
2023-03-21 19:05 Gonosomal dominant inheritance Jowel Jbara Original text is from WikiSkripta (https://www.wikiskripta.eu/index.php?curid=1052)


Explanatory Notes
Flags: me - minor edit, d - deleted.