Category:Medical genetics task force articles
Subcategories
This category has the following 2 subcategories, out of 2 total.
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)0–9
- Talk:1p36 deletion syndrome
- Talk:1q21.1 deletion syndrome
- Talk:1q21.1 duplication syndrome
- Talk:2-Hydroxyacid oxidase 2
- Talk:2-Hydroxyglutaric aciduria
- Talk:2-Methylbutyryl-CoA dehydrogenase deficiency
- Talk:2,4 Dienoyl-CoA reductase deficiency
- Talk:2p15-16.1 microdeletion syndrome
- Talk:2q37 deletion syndrome
- Talk:3 hydroxyisobutyric aciduria
- Talk:3-hydroxy-3-methylglutaryl-CoA lyase deficiency
- Talk:3-Hydroxy-3-methylglutaryl-CoA lyase deficiency
- Talk:3-Hydroxyisobutyryl-CoA deacylase deficiency
- Talk:3-M syndrome
- Talk:3-Methylcrotonyl-CoA carboxylase deficiency
- Talk:3-Methylglutaconic aciduria
- Talk:3C syndrome
- Talk:3p deletion syndrome
- Talk:5,10-methenyltetrahydrofolate synthetase deficiency
- Talk:6-phosphogluconate dehydrogenase deficiency
- Talk:6-Pyruvoyltetrahydropterin synthase deficiency
- Talk:7q11.23 duplication syndrome
- Talk:9q34.3 deletion syndrome
- Talk:10q26 deletion
- Talk:13q deletion syndrome
- Talk:16p11.2 deletion syndrome
- Talk:16p11.2 duplication syndrome
- Talk:17q12 microdeletion syndrome
- Talk:17q12 microduplication syndrome
- Talk:18p-
- Talk:22q11.2 distal deletion syndrome
- Talk:22q11.2 duplication syndrome
- Talk:22q13 deletion syndrome
- Talk:23andMe
- Talk:45,X/46,XY mosaicism
- Talk:46,XX/46,XY
- Talk:47,XXY
- Talk:100,000 Genomes Project
A
- Category talk:A-Class medical genetics articles
- Talk:Aacyl CoAoxidase deficiency
- Talk:Aagenaes syndrome
- Talk:Aase syndrome
- Talk:ABCB5
- Talk:ABCD syndrome
- Talk:Abderhalden–Kaufmann–Lignac syndrome
- Talk:Abetalipoproteinemia
- Talk:Ablepharon macrostomia syndrome
- Talk:Absence deformity of leg-cataract syndrome
- Talk:Acatalasia
- Talk:Aceruloplasminemia
- Talk:Achondrogenesis
- Talk:Achondrogenesis type 1B
- Talk:Achondrogenesis type 2
- Talk:Achondroplasia
- Talk:Achondroplasia in children
- Talk:Achromatopsia
- Talk:Acorea, microphthalmia and cataract syndrome
- Talk:Acro-oto-radial syndrome
- Talk:Acrocraniofacial dysostosis
- Talk:Acrodermatitis enteropathica
- Talk:Acrokeratosis verruciformis
- Category talk:Actors with Down syndrome
- Talk:Acute fatty liver of pregnancy
- Talk:Acute necrotizing encephalopathy
- Talk:Acyanotic heart defect
- Talk:Acyl-CoA oxidase deficiency
- Talk:Adams–Oliver syndrome
- Talk:Adducted thumb syndrome
- Talk:Adenine phosphoribosyltransferase deficiency
- Talk:Adenosine deaminase 2 deficiency
- Talk:Adenosine deaminase deficiency
- Talk:Adenylosuccinate lyase deficiency
- Talk:Adermatoglyphia
- Talk:Adrenal hypoplasia
- Talk:Adrenal hypoplasia congenita
- Talk:Adrenal hypoplasia congenital, X-linked
- Talk:Adrenoleukodystrophy
- Talk:Advanced Therapy Medicinal Product
- Talk:African Centre of Excellence for Genomics of Infectious Diseases
- Talk:African iron overload
- Talk:Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome
- Talk:Agenesis
- Talk:AHDC1
- Talk:Nadav Ahituv
- Talk:Aicardi syndrome
- Talk:Aicardi–Goutières syndrome
- Talk:Al Gazali Sabrinathan Nair syndrome
- Talk:Alagille syndrome
- Category talk:Albinism
- Talk:Albinism in humans
- Category talk:Albinism organizations
- Talk:Alder–Reilly anomaly
- Talk:Aldolase A deficiency
- Talk:Alexander disease
- Talk:ALG1-CDG
- Talk:Alkaptonuria
- Talk:Allele chart
- Talk:Allelic heterogeneity
- Talk:Alpha-1 antitrypsin deficiency
- Talk:Alpha-mannosidosis
- Talk:Alport syndrome
- Talk:Alström syndrome
- Talk:Alternating hemiplegia of childhood
- Talk:Amaurosis congenita, cone-rod type, with congenital hypertrichosis
- Talk:Amelogenesis imperfecta
- Talk:Aminoacylase 1 deficiency
- Talk:Amish lethal microcephaly
- Category talk:Congenital amputees
- Talk:Andersen–Tawil syndrome
- Talk:Androgen insensitivity syndrome
- Talk:Aneuploidy
- Talk:Angel-shaped phalango-epiphyseal dysplasia
- Talk:Angelman syndrome
- Talk:Angelman's syndrome
- Talk:Anonychia-onychodystrophy with brachydactyly type B and ectrodactyly
- Talk:Antagonistic pleiotropy hypothesis
- Talk:Anticipation (genetics)
- Talk:Aortic arch anomaly - peculiar facies - intellectual disability
- Talk:Aortopulmonary septal defect
- Talk:APECED
- Talk:Apert syndrome
- Talk:Aphalangy-syndactyly-microcephaly syndrome
- Talk:Apparent mineralocorticoid excess syndrome
- Talk:Applications of pcr
- Talk:Applications of PCR
- Talk:Arakawa's syndrome II
- Talk:Arginemia
- Talk:Argininosuccinic aciduria
- Talk:Armed Forces DNA Identification Laboratory
- Talk:Aromatase deficiency
- Talk:Array-comparative genomic hybridization
- Talk:Ascertainment bias
- Talk:Ruth Ashery-Padan
- Talk:Asperger
- Talk:Asperger syndrome
- Talk:Hans Asperger
- Talk:Asymmetric crying facies
- Talk:Ataxia–telangiectasia
- Talk:Atelosteogenesis, type II
- Talk:Athabaskan brainstem dysgenesis syndrome
- Talk:ATR-16 syndrome
- Talk:ATR-X syndrome
- Talk:Atrio-digital syndrome
- Talk:Atriodigital dysplasia
- Talk:Autism
- Talk:Autism spectrum
- Talk:Autism and memory
- Category talk:Autism pseudoscience
- Talk:Autism-Europe
- Category talk:Autism-related organizations
- Talk:Autism: The Musical
- Talk:Autophagic vacuolar myopathy
- Talk:Autosomal dominant cerebellar ataxia
- Talk:Autosomal dominant cerebellar ataxia, deafness, and narcolepsy
- Talk:Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome
- Talk:Autosomal dominant nocturnal frontal lobe epilepsy
- Talk:Autosomal dominant polycystic kidney disease
- Talk:Autosomal dominant porencephaly type I
- Talk:Autosomal recessive multiple epiphyseal dysplasia
- Talk:Autosomal recessive tetra-amelia
- Talk:Autosomal recessive tetraamelia
- Category talk:Autosomal trisomies
B
- Category talk:B-Class medical genetics articles
- Talk:Background radiation equivalent time
- Talk:Bainbridge–Ropers syndrome
- Talk:Baller–Gerold syndrome
- Talk:Bannayan–Riley–Ruvalcaba syndrome
- Talk:Banti's syndrome
- Talk:Barakat-Perenthaler syndrome
- Talk:Bardet–Biedl syndrome
- Talk:Bare lymphocyte syndrome
- Talk:Bare lymphocyte syndrome type II
- Talk:Barth syndrome
- Talk:Bartter syndrome
- Talk:Bazex–Dupré–Christol syndrome
- Talk:Becker muscular dystrophy
- Talk:Beckwith–Wiedemann syndrome
- Talk:Behavioural genetics
- Category talk:Behavioural genetics journals
- Category talk:Behavioural genetics societies
- Talk:Behr syndrome
- Talk:BeiGene
- Talk:Benign familial infantile epilepsy
- Talk:Benign familial neonatal seizures
- Talk:Benign hereditary chorea
- Talk:Berdon syndrome
- Talk:Beta thalassemia
- Talk:Beta-ketothiolase deficiency
- Talk:Bifid nose
- Talk:Biliary atresia
- Talk:Binder's syndrome
- Talk:Biological inheritance
- Talk:Biotinidase
- Talk:Biotinidase deficiency
- Talk:Birt–Hogg–Dubé syndrome
- Talk:Blepharophimosis intellectual disability syndromes
- Talk:Blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome
- Talk:Bloom syndrome
- Talk:Blue diaper syndrome
- Talk:Bochdalek hernia