Category:Medical genetics task force articles
Pages in category "Medical genetics task force articles"
The following 200 pages are in this category, out of approximately 1,261 total. This list may not reflect recent changes.
(previous page) (next page)E
- Talk:Ehlers–Danlos syndrome
- Talk:Ellis–Van Creveld syndrome
- Talk:Emery–Dreifuss muscular dystrophy
- Talk:Emily's Entourage
- Talk:Engelmann syndrome
- Talk:Epidemiology of autism
- Talk:Epidermolysis bullosa
- Talk:Epidermolytic hyperkeratosis
- Talk:Epigenetics
- Talk:Epigenetics of anxiety and stress–related disorders
- Talk:Epigenetics of autoimmune disorders
- Talk:Epigenomics
- Talk:Episodic Ataxia Type-1
- Talk:Erythromelalgia
- Talk:Erythropoiesis
- Talk:Erythropoietic protoporphyria
- Talk:Ethylmalonic encephalopathy
- Talk:Examples of PCR
- Talk:Expression quantitative trait loci
- Talk:Expressivity (genetics)
F
- Category talk:FA-Class medical genetics articles
- Talk:Fabry disease
- Talk:Faciocardiorenal syndrome
- Talk:Facioscapulohumeral muscular dystrophy
- Talk:Factor IX
- Talk:Factor V Leiden
- Talk:Factor VIII
- Talk:Factor XI
- Talk:FAD-dependent oxidoreductase domain-containing protein 2
- Talk:Familial adenomatous polyposis
- Talk:Familial Alzheimer disease
- Talk:Familial amyloid polyneuropathy
- Talk:Familial dwarfism and painful muscle spasms
- Talk:Familial dysautonomia
- Talk:Familial episodic pain syndrome
- Talk:Familial hemiplegic migraine
- Talk:Familial isolated vitamin E deficiency
- Talk:Familial Mediterranean fever
- Talk:Familial multiple cafe-au-lait spots
- Talk:Familial nasal acilia
- Talk:Familial opposable triphalangeal thumbs duplication
- Talk:Familial osteodysplasia, Anderson type
- Talk:Familial thoracic aortic aneurysm and aortic dissection
- Talk:Family aggregation
- Talk:Fanconi anemia
- Talk:Alessio Fasano
- Talk:Fazio–Londe disease
- Talk:FBXW7 neurodevelopmental syndrome
- Talk:Feigenbaum-Bergeron-Richardson syndrome
- Talk:Feingold syndrome
- Talk:Fetal hydantoin syndrome
- Talk:FG syndrome
- Category talk:People with cystic fibrosis
- Talk:Fibular aplasia-ectrodactyly syndrome
- Talk:Fibular hemimelia
- Category talk:Fictional characters with albinism
- Category talk:Films about sex selection in India
- Talk:Fine–Lubinsky syndrome
- Category talk:FL-Class medical genetics articles
- Talk:Floating–Harbor syndrome
- Talk:Flynn–Aird syndrome
- Talk:JoAnne Flynn
- Talk:Focal facial dermal dysplasia
- Talk:Follicle-stimulating hormone insensitivity
- Talk:FOSB
- Talk:Fragile X syndrome
- Talk:Fraser syndrome
- Talk:Frasier syndrome
- Talk:Joseph F. Fraumeni Jr.
- Talk:Kelly A. Frazer
- Talk:Brendan Frey
- Talk:Frontotemporal dementia and parkinsonism linked to chromosome 17
- Talk:Fructose malabsorption
- Talk:Fryns syndrome
- Talk:Fukuyama congenital muscular dystrophy
G
- Talk:G protein-coupled receptor kinase 3
- Category talk:GA-Class medical genetics articles
- Talk:Galactosemia
- Talk:Galactosialidosis
- Talk:Ayelet Galena
- Talk:Galloway–Mowat syndrome
- Talk:Gamma-aminobutyric acid receptor-associated protein-like 1
- Talk:GAPO syndrome
- Talk:Gardner's syndrome
- Talk:Garrod's tetrad
- Talk:GATAD2B-associated neurodevelopmental disorder
- Talk:Gaucher's disease
- Talk:Gene delivery
- Talk:Gene Diagnostics
- Talk:Gene duplication
- Category talk:Gene tests
- Talk:Gene therapy
- Talk:Gene therapy for color blindness
- Talk:Gene therapy for Duchenne muscular dsytrophy
- Talk:Gene therapy for epilepsy
- Talk:Gene therapy for osteoarthritis
- Talk:Gene therapy in Parkinson's disease
- Talk:Gene Wiki
- Talk:Gene–environment interaction
- Talk:GeneMatcher
- Talk:Genes, Brain and Behavior
- Talk:Genetic counseling
- Category talk:Genetic disease and disorder templates by mechanism
- Talk:Genetic disorder
- Category talk:Genetic disorders by inheritance
- Category talk:Genetic disorders with known gene but no known gene function
- Talk:Genetic epidemiology
- Talk:Genetic exceptionalism
- Talk:Genetic heterogeneity
- Talk:Genetic linkage
- Talk:Genetic marker
- Talk:Genetic screen
- Talk:Genetic testing
- Category talk:Genetics
- Talk:Genetics
- Category talk:Genetics journal stubs
- Talk:Genetics of aging
- Talk:Genetics of Down syndrome
- Talk:Genetics of infertility
- Talk:Genetics of obesity
- Talk:Genetics of social behavior
- Category talk:Genetics societies
- Category talk:Genetics terms
- Talk:Geniom RT Analyzer
- Talk:Genitopatellar syndrome
- Talk:Genodermatosis
- Talk:Genome-wide association study
- Talk:Genomic counseling
- Talk:Genomic imprinting
- Talk:Genomics
- Talk:Genomics England
- Talk:Deborah German
- Talk:Germline mosaicism
- Talk:Germline mutation
- Talk:Giant axonal neuropathy
- Talk:Gilbert's syndrome
- Talk:Gitelman syndrome
- Talk:Glanzmann's thrombasthenia
- Talk:Generalized glucocorticoid resistance
- Talk:Glutaric acidemia type 2
- Talk:Glutaric aciduria type 1
- Talk:Gluten immunochemistry
- Talk:Gluten-sensitive idiopathic neuropathies
- Talk:Glycogen storage disease type I
- Talk:Glycogen storage disease type II
- Talk:Glycogen storage disease type III
- Talk:Glycogen storage disease type IX
- Talk:Glycogen storage disease type VI
- Talk:GM2 gangliosidoses
- Talk:GM2-gangliosidosis, AB variant
- Talk:GNE (gene)
- Talk:Gonadotropin-releasing hormone insensitivity
- Talk:GRACILE syndrome
- Talk:Grebe chondrodysplasia
- Talk:Greig cephalopolysyndactyly syndrome
- Talk:Growth delay-hydrocephaly-lung hypoplasia syndrome
- Talk:Gulf War syndrome
- Talk:Gustavson syndrome
- Talk:Robert Guthrie (microbiologist)
- Talk:Mitchell Guttman
H
- Talk:Haemophilia
- Talk:Haemophilia A
- Talk:Haemophilia B
- Talk:Haemophilia C
- Talk:Haemophilia in European royalty
- Talk:Hajdu–Cheney syndrome
- Talk:Half-identical twin
- Talk:Hallermann–Streiff syndrome
- Talk:Halperin-Birk syndrome
- Talk:Happy puppet syndrome
- Talk:Harlequin-type ichthyosis
- Talk:Hawkinsinuria
- Talk:Health aspects of Down syndrome
- Talk:Healthcare scientist
- Talk:Heart-hand syndrome, Spanish type
- Talk:Heart-hand syndrome, type 1
- Talk:Heimler syndrome
- Talk:Hemimelia
- Talk:Hemiplegic migraine
- Talk:Hemoglobin Hopkins-2
- Talk:Hennekam syndrome
- Talk:Hereditary cystatin C amyloid angiopathy
- Talk:Hereditary Disease Foundation
- Talk:Hereditary elliptocytosis
- Talk:Hereditary fructose intolerance
- Talk:Hereditary haemochromatosis
- Talk:Hereditary hemorrhagic telangiectasia
- Talk:Hereditary inclusion body myopathy
- Talk:Hereditary lobular breast cancer
- Talk:Hereditary motor and sensory neuropathy
- Talk:Hereditary multiple exostoses
- Talk:Hereditary nonpolyposis colorectal cancer
- Talk:Hereditary pancreatitis
- Talk:Hereditary spastic paraplegia
- Talk:Hereditary stomatocytosis
- Talk:Heredity in Relation to Eugenics
- Talk:Heritability
- Talk:Heritability of autism
- Talk:Heteroplasmy
- Talk:High-arched palate