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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- 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
- Talk:Diagnosis of autism
- Talk:Diagnostic Interview for Genetic Studies
- Talk:Diamond–Blackfan anemia
- Talk:Diastrophic dysplasia
- Talk:DiGeorge syndrome
- Talk:Dihydrofolate reductase deficiency
- Talk:Dihydropteridine reductase deficiency
- Talk:Dihydropyrimidine dehydrogenase deficiency
- Category talk:Disambig-Class medical genetics articles
- Category talk:Deaths from Crohn's disease
- Category talk:People with Huntington's disease
- Talk:Distal hereditary motor neuronopathies
- Talk:Distal intestinal obstruction syndrome
- Talk:Distal myopathy
- Talk:Distal spinal muscular atrophy type 1
- Talk:Distal trisomy 10q
- Category talk:Disturbances of pigmentation
- Talk:DNA condensation
- Talk:DNA digital data storage
- Talk:DNA repair-deficiency disorder
- Talk:Dolichonychia
- Talk:DOOR syndrome
- Talk:Dor Yeshorim
- Talk:Down syndrome
- Category talk:Down syndrome in film
- Talk:Du Pan syndrome
- Talk:Duane syndrome
- Talk:Duane-radial ray syndrome
- Talk:Duchenne dystrophy
- Talk:Duchenne muscular dystrophy
- Talk:Duchenne Muscular Dystrophy
- Talk:Duchenne type muscular dystrophy
- Talk:Duchenne's muscle dystrophy
- Talk:Duchenne's muscular dystrophy
- Talk:Duchenne's Muscular Dystrophy
- Talk:Duchenne’s muscular dystrophy
- Talk:Duchenne’s Muscular Dystrophy
- Talk:Duchennes Muscular Distrophy
- Talk:Sandrine Dudoit
- Talk:Dup15q
- Talk:Dwarfism, low-birth-weight type with unresponsiveness to growth hormone
- Talk:Dysferlinopathy
- Talk:Dystrophin
- Talk:Dystrophin mutation
E
- Talk:Ectrodactyly
- Talk:Ectrodactyly with tibia aplasia/hypoplasia
- Talk:Ectrodactyly-polydactyly syndrome
- Talk:Ehlers–Danlos syndrome
- Talk:Ellis–Van Creveld syndrome
- Talk:Emery–Dreifuss muscular dystrophy
- Talk:Emily's Entourage
- Talk:Engelmann syndrome
- Talk:Epidemiology of autism
- Talk:Epidermolysis bullosa
- Talk:Epidermolytic hyperkeratosis
- Talk:Epigenetics
- Talk:Epigenetics of anxiety and stress–related disorders
- Talk:Epigenetics of autoimmune disorders
- Talk:Epigenomics
- Talk:Episodic Ataxia Type-1
- Talk:Erythromelalgia
- Talk:Erythropoiesis
- Talk:Erythropoietic protoporphyria
- Talk:Ethylmalonic encephalopathy
- Talk:Examples of PCR
- Talk:Expression quantitative trait loci
- Talk:Expressivity (genetics)
F
- Category talk:FA-Class medical genetics articles
- Talk:Fabry disease
- Talk:Faciocardiorenal syndrome
- Talk:Facioscapulohumeral muscular dystrophy
- Talk:Factor IX
- Talk:Factor V Leiden
- Talk:Factor VIII
- Talk:Factor XI
- Talk:Familial adenomatous polyposis
- Talk:Familial Alzheimer disease
- Talk:Familial amyloid polyneuropathy
- Talk:Familial dwarfism and painful muscle spasms
- Talk:Familial dysautonomia
- Talk:Familial episodic pain syndrome
- Talk:Familial hemiplegic migraine
- Talk:Familial isolated vitamin E deficiency
- Talk:Familial Mediterranean fever
- Talk:Familial multiple cafe-au-lait spots
- Talk:Familial nasal acilia
- Talk:Familial opposable triphalangeal thumbs duplication
- Talk:Familial osteodysplasia, Anderson type
- Talk:Familial thoracic aortic aneurysm and aortic dissection
- Talk:Family aggregation
- Talk:Fanconi anemia
- Talk:Alessio Fasano
- Talk:Fazio–Londe disease
- Talk:FBXW7 neurodevelopmental syndrome
- Talk:Feigenbaum-Bergeron-Richardson syndrome
- Talk:Feingold syndrome
- Talk:David S. Feldman
- Talk:Fetal hydantoin syndrome
- Talk:FG syndrome
- Category talk:People with cystic fibrosis
- Talk:Fibular aplasia-ectrodactyly syndrome
- Talk:Fibular hemimelia
- Category talk:Fictional characters with albinism
- Category talk:Films about sex selection in India
- Talk:Fine–Lubinsky syndrome
- Category talk:FL-Class medical genetics articles
- Talk:Floating–Harbor syndrome
- Talk:Flynn–Aird syndrome
- Talk:JoAnne Flynn
- Talk:Focal facial dermal dysplasia
- Talk:Follicle-stimulating hormone insensitivity
- Talk:FOSB
- Talk:Fragile X syndrome