Category:Start-Class medical genetics articles
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| 3 | 0 | 22 | 155 | 287 | 440 | 148 | 0 | 11 | 81 | 2 | 1 | 4 | 105 | 1 | 0 | 0 |
Pages in category "Start-Class medical genetics articles"
The following 200 pages are in this category, out of approximately 440 total. This list may not reflect recent changes.
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F
- Talk:Factor IX
- Talk:Factor VIII
- Talk:Factor XI
- Talk:Familial amyloid polyneuropathy
- Talk:Familial episodic pain syndrome
- Talk:Familial isolated vitamin E deficiency
- Talk:Familial multiple cafe-au-lait spots
- Talk:Familial osteodysplasia, Anderson type
- Talk:Familial thoracic aortic aneurysm and aortic dissection
- Talk:Family aggregation
- Talk:Fazio–Londe disease
- Talk:FBXW7 neurodevelopmental syndrome
- Talk:Feingold syndrome
- Talk:Fetal hydantoin syndrome
- Talk:FG syndrome
- Talk:Fibular hemimelia
- Talk:Fine–Lubinsky syndrome
- Talk:Flynn–Aird syndrome
- Talk:JoAnne Flynn
- Talk:Follicle-stimulating hormone insensitivity
- Talk:Frasier syndrome
- Talk:Joseph F. Fraumeni Jr.
G
- Talk:G protein-coupled receptor kinase 3
- Talk:Galloway–Mowat syndrome
- Talk:GAPO syndrome
- Talk:Gardner's syndrome
- Talk:GATAD2B-associated neurodevelopmental disorder
- Talk:Gene Wiki
- Talk:Gene–environment interaction
- Talk:GeneMatcher
- Talk:Genetic screen
- Talk:Genetics of aging
- Talk:Genetics of infertility
- Talk:Genetics of obesity
- Talk:Geniom RT Analyzer
- Talk:Genitopatellar syndrome
- Talk:Genomic counseling
- Talk:Genomics England
- Talk:Deborah German
- Talk:Giant axonal neuropathy
- Talk:Glanzmann's thrombasthenia
- Talk:Glutaric acidemia type 2
- Talk:Glycogen storage disease type VI
- Talk:GM2 gangliosidoses
- Talk:GRACILE syndrome
- Talk:Greig cephalopolysyndactyly syndrome
- Talk:Growth delay-hydrocephaly-lung hypoplasia syndrome
- Talk:Gustavson syndrome
- Talk:Robert Guthrie (microbiologist)
- Talk:Mitchell Guttman
H
- Talk:Hallermann–Streiff syndrome
- Talk:Healthcare scientist
- Talk:Heart-hand syndrome, Spanish type
- Talk:Heimler syndrome
- Talk:Hemimelia
- Talk:Hemiplegic migraine
- Talk:Hennekam syndrome
- Talk:Hereditary cystatin C amyloid angiopathy
- Talk:Hereditary lobular breast cancer
- Talk:Hereditary stomatocytosis
- Talk:Heritability of autism
- Talk:High-arched palate
- Talk:HITS-CLIP
- Talk:HLA-DQB1
- Talk:John Holloway (geneticist)
- Talk:Holocarboxylase synthetase deficiency
- Talk:Holt–Oram syndrome
- Talk:Human genetics
- Talk:Human Heredity and Health in Africa
- Talk:Huntingtin-interacting protein 1
- Talk:Huntington's disease-like syndrome
- Talk:HUPRA syndrome
- Talk:Hyperglycerolemia
- Talk:Hyperkalemic periodic paralysis
- Talk:Hypochondrogenesis
- Talk:Hypohidrotic ectodermal dysplasia
- Talk:Hypomagnesemia with secondary hypocalcemia
- Talk:Hypotrichosis with juvenile macular dystrophy
I
- Talk:I-cell disease
- Talk:Ichthyosis vulgaris
- Talk:Immunodeficiency–centromeric instability–facial anomalies syndrome
- Talk:Inborn errors of immunity
- Talk:Incontinentia pigmenti
- Talk:Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
- Talk:Interferon-induced transmembrane protein 5
- Talk:Internexin
- Talk:Intraepithelial lymphocyte
- Talk:Isobutyryl-coenzyme A dehydrogenase deficiency
- Talk:Isogenic human disease models
- Talk:Isovaleric acidemia
J
K
L
- Talk:Langer–Giedion syndrome
- Talk:Laurence–Moon syndrome
- Talk:Leukocyte adhesion deficiency
- Talk:Leukocyte adhesion deficiency-1
- Talk:Leydig cell hypoplasia
- Talk:Li–Fraumeni syndrome
- Talk:Liddle's syndrome
- Talk:Lipid storage disorder
- Talk:Loeys–Dietz syndrome
- Talk:Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
- Talk:Long-term nonprogressor
- Talk:Low copy repeats
- Talk:Luscan-Lumish syndrome
- Talk:Lysinuric protein intolerance
M
- Talk:Mahvash disease
- Talk:Major histocompatibility complex, class II, DQ alpha 1
- Talk:Malonic aciduria
- Talk:Mannosidosis
- Talk:Maple syrup urine disease
- Talk:McCune–Albright syndrome
- Talk:McGillivray syndrome
- Talk:McKusick–Kaufman syndrome
- Talk:McLeod syndrome
- Talk:Meacham syndrome
- Talk:Medical genetics of Jews
- Talk:Meromelia
- Talk:Metachromatic leukodystrophy
- Talk:Microcephalic primordial dwarfism, Montreal type
- Talk:Microcephaly lymphoedema chorioretinal dysplasia
- Talk:Microcytic anemia
- Talk:Microdeletion syndrome
- Talk:Minor physical anomalies
- Talk:Mir-663 microRNA precursor family
- Talk:Mir-708 microRNA precursor family
- Talk:Mismatch repair cancer syndrome
- Talk:Missing heritability problem
- Talk:Mitochondrial complex II deficiency
- Talk:Molybdenum cofactor deficiency
- Talk:MOMO syndrome
- Talk:Mongolian idiocy
- Talk:Mosaic loss of chromosome Y
- Talk:Roxana Moslehi
- Talk:Mouse models of Down syndrome
- Talk:Mucolipidosis
- Talk:Multifactorial disease
- Talk:Multifocal stenosing ulceration of the small intestine
- Talk:Multiple congenital anomalies-hypotonia-seizures syndrome
- Talk:Multiple endocrine neoplasia type 1
- Talk:Multiple endocrine neoplasia type 2
- Talk:Multiple sulfatase deficiency
- Talk:MUTYH-associated polyposis
- Talk:Myopathy
- Talk:Myopathy, X-linked, with excessive autophagy
- Talk:Myotonia congenita
N
- Talk:N-Acetylglutamate synthase deficiency
- Talk:Nail–patella syndrome
- Talk:Nance–Horan syndrome
- Talk:National Bleeding Disorders Foundation
- Talk:National Society of Genetic Counselors
- Talk:Nemaline myopathy
- Talk:Neonatal hemochromatosis
- Talk:Neonatal teeth
- Talk:Neotenic complex syndrome
- Talk:Nijmegen breakage syndrome
- Talk:Noninvasive prenatal testing
- Talk:Novartis Gene Therapies
- Talk:Nuclear gene
- Talk:Nuclear protein in testis gene
- Talk:Nucleotide salvage
O
- Talk:Occipital horn syndrome
- Talk:Ocular albinism
- Talk:Oculocutaneous albinism
- Talk:Oculodentodigital dysplasia
- Talk:Odontoma dysphagia syndrome
- Talk:Omenn syndrome
- Talk:Ornithine aminotransferase deficiency
- Talk:Osimertinib
- Talk:Osteopathia striata with cranial sclerosis
- Talk:Oto-palato-digital syndrome
- Talk:Otospondylomegaepiphyseal dysplasia
P
- Talk:Pallister–Hall syndrome
- Talk:Pallister–Killian syndrome
- Talk:Paramutation
- Talk:Paternal mtDNA transmission
- Talk:Pelizaeus–Merzbacher disease
- Talk:Periodic paralysis
- Talk:Perlman syndrome
- Talk:Persistent Müllerian duct syndrome
- Talk:Peters-plus syndrome
- Talk:Pfeiffer syndrome
- Talk:Pharmacogenomics
- Talk:Pierre Robin sequence