Category:Medical genetics task force articles
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Pages in category "Medical genetics task force articles"
The following 200 pages are in this category, out of approximately 1,234 total. This list may not reflect recent changes.
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- 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
- 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: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: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:Cri du chat syndrome
- Talk:Crigler–Najjar syndrome
- 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
- Talk:Dentinogenesis imperfecta
- Talk:Denys–Drash syndrome
- Talk:Desmin-related myofibrillar myopathy
- Talk:Developmental coordination disorder
- Talk:Dextrocardia
- Talk:Diagnosis of Asperger syndrome