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.
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- 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
- Category talk:High-importance medical genetics articles
- Talk:Hirschsprung's disease
- Talk:Hirschsprung's disease-type D brachydactyly syndrome
- Talk:History of Asperger syndrome
- Talk:History of Tay–Sachs disease
- Talk:HITS-CLIP
- Talk:HLA-DQ1
- Talk:HLA-DQB1
- Talk:Niels Høiby
- Talk:Andrew Holding
- Talk:John Holloway (geneticist)
- Talk:Holocarboxylase synthetase deficiency
- Talk:Holt oram
- Talk:Holt oram syndrome
- Talk:Holt Oram Syndrome
- Talk:Holt-Oram syndrome
- Talk:Holt-Oram Syndrome
- Talk:Holt–Oram syndrome
- Talk:Homocystinuria
- Talk:Hot-start
- Talk:Human behaviour genetics
- Talk:Human disease modifier gene
- Talk:Human genetics
- Talk:Human Heredity and Health in Africa
- File talk:Human karyotype with bands and sub-bands.png
- Talk:Hunter syndrome
- Talk:Huntingtin-interacting protein 1
- Talk:Huntington's disease
- Category talk:Huntington's disease
- Talk:Huntington's disease clinical research
- Talk:Huntington's disease-like syndrome
- Talk:HUPRA syndrome
- Talk:Hurler syndrome
- Talk:Hyper-IgD syndrome
- Talk:Hyperglycerolemia
- Talk:Hyperkalemic periodic paralysis
- Talk:Hypochondrogenesis
- Talk:Hypochondroplasia
- Talk:Hypohidrotic ectodermal dysplasia
- Talk:Hypokalemic periodic paralysis
- Talk:Hypomagnesemia with secondary hypocalcemia
- Talk:Hypotrichosis with juvenile macular dystrophy
I
- Talk:I-cell disease
- Talk:Ichthyosis vulgaris
- Talk:Ichthyosis-intellectual disability-dwarfism-renal impairment
- Talk:Immunodeficiency–centromeric instability–facial anomalies syndrome
- Talk:Inborn error of lipid metabolism
- Talk:Inborn errors of immunity
- Talk:Inborn errors of metabolism
- Talk:Inbreeding
- Talk:Inclusion body myositis
- Talk:Incontinentia pigmenti
- Talk:Indian childhood cirrhosis
- Category talk:Indian molecular biologists
- Talk:Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
- Talk:Infantile cortical hyperostosis
- Talk:Infantile spasms-broad thumbs syndrome
- Category talk:Inflammatory bowel disease
- Talk:Inflammatory bowel disease
- Talk:Intellectual disability-spasticity-ectrodactyly syndrome
- Talk:Interferon-induced transmembrane protein 5
- Talk:Interleukin-1 receptor-associated kinase 1-binding protein 1
- Talk:Internexin
- Talk:Intraepithelial lymphocyte
- Talk:Iris hypoplasia with glaucoma
- Talk:Isobutyryl-coenzyme A dehydrogenase deficiency
- Talk:Isodicentric 15
- Talk:Isogenic human disease models
- Talk:Isolated growth hormone deficiency
- Talk:Isovaleric acidemia
- Category talk:Italian molecular biologists