Category:Start-Class medical genetics articles
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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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- Talk:Background radiation equivalent time
- Talk:Bainbridge–Ropers syndrome
- Talk:Baller–Gerold syndrome
- Talk:Banti's syndrome
- Talk:Barakat-Perenthaler syndrome
- Talk:Bare lymphocyte syndrome
- Talk:Barth syndrome
- Talk:Bazex–Dupré–Christol syndrome
- Talk:Behr syndrome
- Talk:Benign familial infantile epilepsy
- Talk:Berdon syndrome
- Talk:Beta-ketothiolase deficiency
- Talk:Biliary atresia
- Talk:Binder's syndrome
- Talk:Biotinidase
- Talk:Biotinidase deficiency
- Talk:Blepharophimosis intellectual disability syndromes
- Talk:Bloom syndrome
- Talk:Blue diaper syndrome
- Talk:Bosch–Boonstra–Schaaf optic atrophy syndrome
- Talk:British Heart Foundation
- Talk:Broad Institute
- Talk:Brody myopathy
- Talk:Peter H. Byers
C
- Talk:Camptodactyly
- Talk:Camptodactyly-arthropathy-coxa vara-pericarditis syndrome
- Talk:Carbamoyl phosphate synthetase I deficiency
- Talk:Cardiofaciocutaneous syndrome
- Talk:Carnitine palmitoyltransferase I deficiency
- Talk:Carnitine-acylcarnitine translocase deficiency
- Talk:Cat eye syndrome
- Talk:CCR2
- Talk:Celera Corporation
- Talk:Central nervous system cavernous hemangioma
- Talk:Cerebellar ataxia, neuropathy, vestibular areflexia syndrome
- Talk:Cerebro-costo-mandibular syndrome
- Talk:CHAMP1-associated intellectual disability syndrome
- Talk:Channelopathy
- Talk:Chondrodysplasia, Grebe type
- Talk:Chorionic villus sampling
- Talk:Chromosomal deletion syndrome
- Talk:Chromosomal translocation
- Talk:Chromosome 3
- Talk:Chromosome 4
- Talk:Chromosome 5
- Talk:Chromosome 5q deletion syndrome
- Talk:Chromosome 10
- Talk:Chromosome 11
- Talk:Chromosome 14
- Talk:Chromosome 15q trisomy
- Talk:Chromosome 17
- Talk:Chromosome 18
- Talk:Chromosome 20
- Talk:Chromosome 22
- Talk:Chromosome abnormality
- Talk:Chromosome instability syndrome
- Talk:Chudley–Mccullough syndrome
- Talk:Citrullinemia
- Talk:Classic autism
- Talk:Classical genetics
- Talk:Cleft palate short stature vertebral anomalies syndrome
- Talk:Coffin–Lowry syndrome
- Talk:Cohen syndrome
- Talk:Collagenopathy, types II and XI
- Talk:Complex segregation analysis
- Talk:Congenital dyserythropoietic anemia type I
- Talk:Congenital dyserythropoietic anemia type II
- Talk:Congenital dyserythropoietic anemia type III
- Talk:Congenital dyserythropoietic anemia type IV
- Talk:Congenital pulmonary airway malformation
- Talk:Congenital tufting enteropathy
- Talk:Contiguous gene syndrome
- Talk:Riccardo Cortese
- Talk:Craniodiaphyseal dysplasia
- Talk:Cri du chat syndrome
- Talk:Crouzonodermoskeletal syndrome
- Talk:Cryptotia
- Talk:Cystinosis
- Talk:Cystinuria
D
- Talk:Dauwerse–Peters syndrome
- Talk:De Barsy syndrome
- Talk:DeFries–Fulker regression
- Talk:Deletion (genetics)
- Talk:Denys–Drash syndrome
- Talk:Desmin-related myofibrillar myopathy
- Talk:Dextrocardia
- Talk:Diastrophic dysplasia
- Talk:Dihydropteridine reductase deficiency
- Talk:Dihydropyrimidine dehydrogenase deficiency
- Talk:Distal hereditary motor neuronopathies
- Talk:Distal intestinal obstruction syndrome
- Talk:Distal myopathy
- Talk:Distal trisomy 10q
- Talk:DNA digital data storage
- Talk:DNA repair-deficiency disorder
- Talk:DOOR syndrome
- Talk:Dor Yeshorim
- Talk:Duane-radial ray syndrome
- Talk:Sandrine Dudoit
- Talk:Dysgenics
- Talk:Dystrophin
E
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