Category:C-Class medical genetics articles
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Pages in category "C-Class medical genetics articles"
The following 182 pages are in this category, out of approximately 284 total. This list may not reflect recent changes.
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F
- Talk:Fabry disease
- Talk:Factor V Leiden
- Talk:Familial dysautonomia
- Talk:Familial Mediterranean fever
- Talk:Familial opposable triphalangeal thumbs duplication
- Talk:Fanconi anemia
- Talk:Alessio Fasano
- Talk:Floating–Harbor syndrome
- Talk:Focal facial dermal dysplasia
- Talk:FOSB
- Talk:Fraser syndrome
- Talk:Frontotemporal dementia and parkinsonism linked to chromosome 17
- Talk:Fryns syndrome
- Talk:Fukuyama congenital muscular dystrophy
G
- Talk:Galactosemia
- Talk:Galactosialidosis
- Talk:Ayelet Galena
- Talk:Gene duplication
- Talk:Gene therapy for color blindness
- Talk:Gene therapy for epilepsy
- Talk:Gene therapy in Parkinson's disease
- Talk:Genetic counseling
- Talk:Genetic epidemiology
- Talk:Genetic marker
- Talk:Genodermatosis
- Talk:Germline mosaicism
- Talk:Gilbert's syndrome
- 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:Gonadotropin-releasing hormone insensitivity
H
- Talk:Haemophilia
- Talk:Haemophilia B
- Talk:Haemophilia C
- Talk:Haemophilia in European royalty
- Talk:Hajdu–Cheney syndrome
- Talk:Halperin-Birk syndrome
- Talk:Harlequin-type ichthyosis
- Talk:Hemoglobin Hopkins-2
- Talk:Hereditary fructose intolerance
- Talk:Hereditary inclusion body myopathy
- Talk:Hereditary motor and sensory neuropathy
- Talk:Hereditary multiple exostoses
- Talk:Hereditary nonpolyposis colorectal cancer
- Talk:Hereditary pancreatitis
- Talk:Hereditary spastic paraplegia
- Talk:Heteroplasmy
- Talk:Hirschsprung's disease
- Talk:History of Tay–Sachs disease
- Talk:Andrew Holding
- Talk:Homocystinuria
- Talk:Human behaviour genetics
- Talk:Human disease modifier gene
- Talk:Hunter syndrome
- Talk:Hurler syndrome
- Talk:Hypochondroplasia
- Talk:Hypokalemic periodic paralysis
I
K
L
M
- Talk:Madelung's deformity
- Talk:Mandibulofacial dysostosis-microcephaly syndrome
- Talk:Michelle Maykin
- Talk:MERRF syndrome
- Talk:Metachondromatosis
- Talk:Microcephaly
- Talk:Microchimerism
- Talk:Miller–Dieker syndrome
- Talk:Mitochondrial biogenesis
- Talk:Mitochondrial disease
- Talk:Mitochondrial trifunctional protein deficiency
- Talk:Moebius syndrome
- Talk:Molecular biology
- Talk:MORM syndrome
- Talk:Mulibrey nanism
- Talk:Muscular Dystrophy Association
- Talk:Myotonic dystrophy
N
P
- Talk:Pancreaticobiliary maljunction
- Talk:PANO1
- Talk:Paramyotonia congenita
- Talk:Patau syndrome
- Talk:Pendred syndrome
- Talk:Penetrance
- Talk:Personalized onco-genomics
- Talk:Peutz–Jeghers syndrome
- Talk:Phenylalanine hydroxylase
- Talk:Philadelphia chromosome
- Talk:Photic sneeze reflex
- Talk:Ploidy
- Talk:Polydactyly
- Talk:Potocki–Lupski syndrome
- Talk:Prenatal testing
- Talk:Primary ciliary dyskinesia
- Talk:Primary familial brain calcification
- Talk:Progerin
- Talk:Pseudocholinesterase deficiency
- Talk:Pseudodeficiency alleles
- Talk:Pyruvate dehydrogenase deficiency
- Talk:Pyruvate kinase deficiency
R
S
- Talk:Sack–Barabas syndrome
- Talk:Saethre–Chotzen syndrome
- Talk:Saito–Kuba–Tsuruta syndrome
- Talk:Sandhoff disease
- Talk:Say–Meyer syndrome
- Talk:Selenium in biology
- Talk:Sex selection
- Talk:Sex-determining region Y protein
- Talk:Short-chain acyl-coenzyme A dehydrogenase deficiency
- Talk:Smith–Fineman–Myers syndrome
- Talk:Smith–Magenis syndrome
- Talk:SMPD1-associated Niemann–Pick disease
- Talk:Sonoda syndrome
- Talk:SPG15 (disease)
- Talk:Spinal and bulbar muscular atrophy
- Talk:Syndromic autism