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: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
- Talk:Bosch–Boonstra–Schaaf optic atrophy syndrome
- Talk:Boudhina-Yedes-Khiari syndrome
- Talk:Brachial amelia, cleft lip, and holoprosencephaly
- Talk:Brachydactyly-long thumb syndrome
- Talk:BRISC and BRCA1-A complex member 2
- Talk:British Heart Foundation
- Talk:Broad Institute
- Talk:Brody myopathy
- Talk:Brown–Vialetto–Van Laere syndrome
- Talk:Brugada syndrome
- Talk:Peter H. Byers
- Talk:Ed Byrne (neuroscientist)
C
- Category talk:C-Class medical genetics articles
- Talk:CADASIL
- Talk:Cadastral gene
- Talk:Camera–Marugo–Cohen syndrome
- Talk:Camptodactyly
- Talk:Camptodactyly-arthropathy-coxa vara-pericarditis syndrome
- Talk:Camptodactyly-taurinuria syndrome
- Talk:Camurati–Engelmann disease
- Talk:Canavan disease
- Talk:Carbamoyl phosphate synthetase I deficiency
- Talk:Cardiac-limb syndrome
- Talk:Cardiofaciocutaneous syndrome
- Talk:William Warrick Cardozo
- Talk:Carnitine palmitoyltransferase I deficiency
- Talk:Carnitine palmitoyltransferase II deficiency
- Talk:Carnitine-acylcarnitine translocase deficiency
- Talk:Carpenter syndrome
- Talk:Carrier testing
- Talk:Cat eye syndrome
- Talk:Cataract-ataxia-deafness syndrome
- Category talk:Category-Class medical genetics articles
- Talk:Cation channel sperm-associated auxiliary subunit beta
- Talk:Cation channel sperm-associated auxiliary subunit delta
- Talk:Cation channel sperm-associated auxiliary subunit gamma
- Talk:Cation channel sperm-associated auxiliary subunit zeta
- Talk:Causes of autism
- Talk:CCR2
- Talk:CCR5
- Talk:CDKL5 deficiency disorder
- Talk:Celera Corporation
- Talk:Cell-free fetal DNA
- Talk:Central nervous system cavernous hemangioma
- Talk:Cerebellar ataxia, neuropathy, vestibular areflexia syndrome
- Talk:Cerebro-costo-mandibular syndrome
- Talk:Cerebrotendinous xanthomatosis
- Talk:CHAMP1-associated intellectual disability syndrome
- Talk:Channelopathy
- Talk:Charcot–Marie–Tooth disease
- Talk:CHCHD10
- Talk:Childhood absence epilepsy
- Talk:Chondrodysplasia, Grebe type
- Talk:Chorionic villus sampling
- Template talk:Chromosomal abnormalities
- Talk:Chromosomal deletion syndrome
- Talk:Chromosomal translocation
- Talk:Chromosome 1
- Talk:Chromosome 2
- 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 partial deletion
- Talk:Chromosome 15q trisomy
- Talk:Chromosome 17
- Talk:Chromosome 18
- Talk:Chromosome 20
- Talk:Chromosome 21
- Talk:Chromosome 22
- Talk:Chromosome abnormality
- Talk:Chromosome instability
- Talk:Chromosome instability syndrome
- Talk:Chronic granulomatous disease
- Talk:Chudley–Mccullough syndrome
- Talk:Ciliopathy
- Talk:Citrullinemia
- Talk:Classic autism
- Talk:Classical genetics
- Talk:Cleft hand
- Talk:Cleft palate short stature vertebral anomalies syndrome
- Talk:Clinic for Special Children
- Talk:Clinodactyly
- Talk:Cockayne syndrome
- Talk:Codon degeneracy
- Talk:Coeliac disease
- Talk:Coeliac UK
- Talk:Coffin–Lowry syndrome
- Talk:Cohen syndrome
- Talk:Collagenopathy, types II and XI
- Talk:Color blindness
- Talk:Colorectal polyp
- Talk:Complete androgen insensitivity syndrome
- Talk:Complex segregation analysis
- Talk:Compound heterozygosity
- Talk:Congenital absence of the fibula
- Talk:Congenital adrenal hyperplasia
- Talk:Congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase deficiency
- Talk:Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
- Talk:Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
- Talk:Congenital adrenal hypoplasia
- Talk:Congenital athymia
- Talk:Congenital disorder of glycosylation
- Talk:Congenital disorder of glycosylation type IIc
- Category talk:Congenital disorders
- Talk:Congenital distal spinal muscular atrophy
- 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 hyperinsulinism
- Talk:Congenital muscular dystrophy
- Talk:Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome
- Talk:Congenital pulmonary airway malformation
- Talk:Congenital tufting enteropathy
- Talk:Conorenal syndrome
- Talk:Contiguous gene syndrome
- Talk:Control of chromosome duplication
- Talk:Copper in biology
- Talk:Copy number variation
- Talk:Cornea plana 1
- Talk:Cornea plana 2
- Talk:Coronary artery anomaly
- Talk:Riccardo Cortese
- Talk:Costello syndrome
- Talk:Cousin syndrome
- Talk:Crandall syndrome
- Talk:Cranio-lenticulo-sutural dysplasia
- Talk:Craniodiaphyseal dysplasia
- Talk:Craniofacial cleft
- Talk:Craniorhiny
- Talk:Cri du chat syndrome
- Talk:Crigler–Najjar syndrome
- Talk:CRISPR gene editing
- Talk:Crisscross heart
- Talk:Crohn's disease
- Category talk:Crohn's disease
- Talk:Crouzon syndrome
- Talk:Crouzonodermoskeletal syndrome
- Talk:Cryptorchidism-arachnodactyly-intellectual disability syndrome
- Talk:Cryptotia
- Talk:Cystic fibrosis
- Talk:Cystic fibrosis transmembrane conductance regulator
- Talk:Cystinosis
- Talk:Cystinuria
- Talk:Cytogenetics
- Category talk:Cytogenetics
D
- Talk:Dauwerse–Peters syndrome
- Talk:De Barsy syndrome
- Talk:De Finetti diagram
- Talk:Deafness-vitiligo-achalasia syndrome
- Category talk:Deaths from cystic fibrosis
- Category talk:Deaths from Huntington's disease
- Category talk:Deaths from muscular dystrophy
- Category talk:Deaths from sickle-cell disease
- Talk:DeFries–Fulker regression
- Talk:Delayed puberty
- Talk:Deletion (genetics)
- Talk:Dent's disease
- Talk:Dentatorubral–pallidoluysian atrophy