Category:Genetics
From WikiLectures
Pages in category "Genetics"
The following 200 pages are in this category, out of 620 total.
(previous page) (next page)A
- A palindrome
- Abnormalities in chromosome number, their causes and clinical presentation in man
- Abnormalities in chromosome structure, their causes and clinical presentation in man
- Adams-Oliver syndrome
- Agglutinogen
- Aims of medical genetics
- Albers-Schönberg Disease
- Albinism
- Alleles
- Allelic interactions
- Alport's syndrome
- Amelogenesis imperfecta
- Ames test
- Amino acid metabolism
- Amniocentesis
- An association study
- Analytical Studies
- Angelman Syndrome
- Angelman syndrome (genetics)
- APC resistance
- Apert syndrome
- Aplasia fibulae congenita
- Aplasia radii congenita
- Apoptosis
- Apoptosis and clinical consequences of disorders of its regulation
- Arabidopsis thaliana
- Arachnodactyly
- Archaea
- Arthrogryposis multiplex congenita
- Assisted Reproduction
- Atypical facial clefts
- Autoimmune diseases
- Autosomal aneuploidy syndromes in man
- Autosomal Disorders
- Autosomal dominant inheritance
- Autosomal dominant inheritance in pedigree and experiment, examples of traits in man
- Autosomal inherited agammaglobulinemia
- Autosomal recessive inheritance
- Autosomal recessive inheritance in pedigree and experiment, examples of traits in man
- Autozomy
B
- Backcross
- Bacteria
- Bacterial chromosome
- Bacterial reproduction
- Bacterial structure
- Bannayan-Riley-Ruvalcaba syndrome
- Bartter syndrome
- Basic components of nucleic acids
- Basic laws of genetics
- Beckwith - Wiedemann Syndrome
- Beckwith-Wiedemann Syndrome
- Binder syndrome
- Biobanks
- Biochemistry of viruses
- Biological properties of tumors
- Portal:Biology and Genetics
- Biology and genetics of viruses, importance in medicine
- Portal:Biology and Genetics/commented links
- Biology of oncogenesis
- Biosynthesis of nucleic acids and proteosynthesis in mitochondria
- Bloch-Sulzberg syndrome
- Bloom's syndrome
- Bond Studies
- BRCA
- Bromouracil
- Bruton's agammaglobulinemia
- Burkitt lymphoma
- Böök syndrome
C
- Caenorhabditis elegans
- Cancer Families
- Carcinogenicity of Substances and Factors in the Environment
- Caring for a child with Down syndrome
- Causes of tumors, carcinogenesis, carcinogens
- Cell and Tissue in vitro Cultivation
- Cell cooperation in the B immune response
- Cell fractionation
- Cell identification
- Cell signalling
- Centromere
- Centromeric index
- Characteristics of cancer cells
- Characteristics of tumour growth
- Charcot-Marie-Tooth Syndrome
- Cherry stain
- Cherry-red spot
- Chiari malformation
- Chorionic Villus Sampling
- Chromatin
- Chromosomal aberrations in cancer cells
- Chromosomal aberrations in the etiology of neoplasms
- Chromosomal Abnormalities
- Chromosomal determination of sex
- Chromosomal sex determination
- Chromosome
- Chromosome aberrations in the etiology of neoplasia
- Chromosome instability syndromes
- Chromosome Number and Structure
- Chronic Granulomatous Disease
- Clastogens
- Cleavage of nucleic acid by hydrolysis
- Cleidocranial dysplasia
- Clinodactyly
- Cloning
- Clubfoot (congenital talipes equinovarus)
- Coefficient of Inbreeding
- Coefficient of Relatedness
- Colcemid
- Colorectal cancer
- Colorectal cancer/screening
- Colorectal carcinoma/screening
- Comparative Genomic Hybridisation
- Comparative genomic hybridization
- Compound heterozygote
- Congenic Strain
- Congenital adrenal hyperplasia
- Congenital defects of the external and middle ear
- Congenital defects of the eye
- Congenital defects of the inner ear
- Congenital defects of the nervous system
- Congenital deformities of the auricle
- Congenital deformities of the neck
- Congenital diaphragmatic hernia
- Congenital disorders of glycosylation
- Congenital Heart Defects
- Congenital limb defects
- Congenital malformations of the auricle
- Congenital malformations of the respiratory system
- Congenital multiple exostoses
- Congenital strain
- Conjugation
- Conjugation, Transformation and Transduction.
- Consomic Strain
- Consomic tribe
- Control of gene expression and proteosynthesis
- Control of gene expression and proteosynthesis in eukaryotes
- Control of gene expression and proteosynthesis in prokaryotes
- Cordocentesis
- Cowden's syndrome
- Craniofacial syndromes
- Crigler-Najjar syndrome
- Crossing-over
- Crossing-over, its mechanism and importance
- Crossing-over, its mechanism and significance
- Crouzon syndrome
- Cutaneous porphyrias
- Cystic Fibrosis
- Cystic fibrosis
- Cystic medial necrosis
- Cystic medionecrosis
D
- Decision-making mechanism for the destruction of non-functional proteins
- DeLange syndrome
- Deletion
- Denaturation of nucleic acids, molecular hybridization
- Dentiogenesis imperfecta
- Description of the Chromosome
- Determination of DNA concentration and purity
- Developmental disorders of the ear
- Developmental hip dysplasia
- Diastrophic dwarfism
- Dihybridism
- Dihybridism, interaction of non-allelic genes, polyhybridism
- Diploid
- Direct diagnosis of hereditary diseases by nucleic acid analysis
- Direct diagnostics of hereditary diseases by nucleic acid analysis
- Disorders of apoptosis signaling in tumor cells
- Disorders of the Sex Chromosomes
- Diversification
- DNA - structure and function
- DNA chips
- DNA cleavage
- DNA Diagnostic Direct Methods
- DNA Diagnostic Indirect Methods
- DNA library
- DNA Methylation
- DNA microarray
- DNA Repair
- Dog equinovarus congenitus
- Down Syndrome
- Drosophila melanogaster
- Duane Retraction Syndrome
- Dubin-johnson syndrome
- Duchenn's muscular atrophy
- Duplication
- Dysostosis cleidocranialis
E
- Ecology, ecogenetics
- Ectodermal dysplasia
- Edwards formula
- Edwards syndrome
- Electrophoresis
- Electrophoresis of nucleic acids
- Enchondromatosis
- Environmental mutagens and teratogens
- Epicanthus
- Epidermolysis bullosa congenita
- Epigenetics
- Ethical and legal aspects of medical genetics
- Ethidium bromide
- Etiology of chromosomal aberrations
- Etiology of Chromosome Abnormalities
Media in category "Genetics"
The following 38 files are in this category, out of 38 total.
AD-Pedigrees.jpg 614 × 635; 42 KB
Amniocentesis.png 800 × 800; 122 KB
AR backcross.jpg 555 × 346; 21 KB
AR experiment.jpg 555 × 346; 21 KB
AR-Pedigrees.jpg 644 × 438; 31 KB
Autosomal dominant inheritance.jpg 438 × 296; 14 KB
Autosomal recessive inheritance.jpg 438 × 296; 14 KB
Backcross in AD.jpg 409 × 234; 13 KB
Cancer syndrome familly.png 428 × 191; 8 KB
Chromosomes structure.png 950 × 603; 17 KB
CONGENIC STRAIN.png 702 × 688; 106 KB
CONSOMIC STRAIN.png 702 × 688; 106 KB
Cordocentesis.png 800 × 800; 114 KB
DihybriddomBc.png 2,396 × 813; 139 KB
DNA with nucleosomes.PNG 800 × 542; 42 KB
DNArepairmech.png 568 × 414; 30 KB
DominantBc.png 1,938 × 1,034; 114 KB
Geneticlinkage.png 1,390 × 1,912; 1.75 MB
Genetics.png 50 × 50; 5 KB
Haplotype.png 380 × 430; 6 KB
Inbreedingcoef.png 1,428 × 1,224; 87 KB
Koeficientpribuznosti.png 1,988 × 1,773; 208 KB
Mutations.png 569 × 374; 31 KB
Pedigree-individuals.png 323 × 248; 29 KB
Pedigree-lines.png 270 × 132; 20 KB
Pedigree-marks.png 282 × 299; 40 KB
RecessiveBc.png 1,947 × 1,034; 111 KB
Retinoblastoma.png 297 × 126; 6 KB
RFLP pedigree.png 343 × 242; 5 KB
Selectiontypes.png 1,968 × 2,238; 278 KB
Standard Deviation.png 819 × 582; 51 KB
Villus sampling.png 800 × 800; 118 KB
X-recessive punnett square.gif 450 × 209; 15 KB
XL-experiment1.jpg 215 × 153; 5 KB
XL-experiment2.jpg 218 × 153; 5 KB
XL-experiment3.jpg 218 × 153; 5 KB
XL-experiment4.jpg 218 × 153; 6 KB
XL-pedigrees.jpg 721 × 514; 35 KB
