Category:Genetics
From WikiLectures
Pages in category "Genetics"
The following 181 pages are in this category, out of 181 total.
A
- Abnormalities in chromosome number, their causes and clinical presentation in man
- Abnormalities in chromosome structure, their causes and clinical presentation in man
- Aims of medical genetics
- Alport's syndrome
- Angelman Syndrome
- Apoptosis
- Archaea
- Autosomal aneuploidy syndromes in man
- Autosomal Disorders
- Autosomal dominant inheritance in pedigree and experiment, examples of traits in man
- Autosomal recessive inheritance in pedigree and experiment, examples of traits in man
B
C
- Cancer Families
- Carcinogenicity of Substances and Factors in the Environment
- Causes of tumors, carcinogenesis, carcinogens
- Cell and Tissue in vitro Cultivation
- Characteristics of cancer cells
- Chorionic Villus Sampling
- Chromosomal aberrations in cancer cells
- Chromosomal Abnormalities
- Chromosomal determination of sex
- Chromosome Number and Structure
- Cloning
- Coefficient of Inbreeding
- Coefficient of Relatedness
- Comparative Genomic Hybridisation
- Congenic Strain
- Conjugation, Transformation and Transduction.
- Consomic Strain
- Cordocentesis
- Crossing-over
- Crossing-over, its mechanism and importance
- Cutaneous porphyrias
- Cystic Fibrosis
D
E
G
- Gametogenesis
- Gametogenesis (Coursebook)
- Gene Expression in Prokaryotes
- Gene Manipulation
- Gene Mutations
- Gene Therapy
- Genealogical method
- Genetic aspects of populations, Hardy-Weinberg equilibrium
- Genetic Code
- Genetic consultation and it importance
- Genetic Counseling
- Genetic determination of body plan in development
- Genetic Drift
- Genetic Liability, Threshold Model.
- Genetic Linkage
- Genetic linkage
- Genetic Linkage Analysis
- Genetic Mapping
- Genetic mapping in man
- Genetic maps and their importance
- Genetics in presymptomatic diagnostics and prevention of cancer
- Genetics of Transplantations
- Genocopy
- Genome
- Genomic Imprinting
- Genotoxic Substances
- Genotype Variation, Mutations and Recombination
- Germ Cell and Somatic Cell Chromosome Mutations
- Germ cell and somatic cell chromosome mutations
- Gilbert Syndrome
- Gonosomal aneuploidy syndromes in man
- Gonosomal inheritance in pedigree and experiment, examples of traits in man
H
I
- Immunocompetent cells
- Inborn errors of development in human, examples, classification
- Inbreeding, Consanguinity and Inherited Diseases
- Indications for Chromosome Analysis
- Indications for chromosome analysis in clinical genetics
- Indirect diagnostics of hereditary diseases by nucleic acid analysis
- Interaction of non-allelic genes
- Inversion
- Isochromosomes
M
O
P
- Patau Syndrome
- Peutz–Jeghers syndrome
- Phenocopy
- Physical mapping of DNA
- Pleiotropy
- Polygenic Inheritance
- Polymerase Chain Reaction
- Polymorphisms of nucleic acids
- Population
- Population Screening
- Postnatal prevention and therapy of heritable and inborn diseases
- Postnatal screening of heritable diseases
- Prader-Willi Syndrome
- Pre-conception prevention of heritable and inborn diseases
- Prenatal Diagnosis of Chromosome Abnormalities
- Prenatal diagnostics of chromosomal aberrations, possibilities of prevention
- Prenatal diagnostics of heritable diseases, possibilities of prevention
- Prenatal diagnostics of inborn errors of development, possibilities of prevention
- Prenatal screening of inborn errors of development
- Prokaryotic Chromosomes
- Protein coding and non-coding sequences of DNA
- Protein Polymorphism
- Proto-oncogenes, oncogenes
- Protooncogenes
R
S
T
- Teratogenesis, teratogens
- The Cell Cycle
- The genetic code
- Transcription, post-transcriptional processing of RNA in eukaryotes
- Translation of membrane and secretory proteins (protein sorting, targeting)
- Translation, post-translational processing of proteins in eukaryotes
- Translocation
- Tumor suppressor genes
- Tumor Supressor Genes
- Turner Syndrome
- Twins and Twin Studies
V
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
