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:Point-of-care genetic testing
- Talk:Polychromia
- Talk:Polydactyly
- Talk:Polydactyly-myopia syndrome
- Talk:Polymerase chain
- Talk:Polymerase Chain Reaction
- Talk:Polymerase chain reaction test
- Talk:Polymerase chain reacton
- Talk:Polymerase proofreading-associated polyposis
- Talk:Pontocerebellar hypoplasia
- Talk:Popliteal pterygium syndrome
- Talk:Porphyria
- Talk:Porphyria cutanea tarda
- Talk:Potocki–Lupski syndrome
- Talk:Potocki–Shaffer syndrome
- Talk:Prader–Willi syndrome
- Talk:Preimplantation genetic diagnosis
- Talk:Preimplantation genetic haplotyping
- Talk:Prenatal testing
- Talk:PRICKLE1-related progressive myoclonus epilepsy with ataxia
- Talk:Primary ciliary dyskinesia
- Talk:Primary familial brain calcification
- Talk:Prime editing
- Talk:Primrose syndrome
- Talk:Proband
- Talk:Proboscis (anomaly)
- Talk:Progeria
- Talk:Progerin
- Talk:Progeroid syndromes
- Talk:Progressive cardiac conduction defect
- Talk:Progressive external ophthalmoplegia
- Talk:Progressive familial intrahepatic cholestasis
- Talk:Progressive pseudorheumatoid dysplasia
- Talk:Propionic acidemia
- Talk:Protein zyg-11 homolog A
- Talk:Prothrombin G20210A
- Talk:Proud syndrome
- Talk:Pseudocholinesterase deficiency
- Talk:Pseudodeficiency alleles
- Talk:Pseudohypertrophic dystrophy
- Talk:PSI (prion)
- Talk:Psychiatric genetics
- Talk:Public health genomics
- Talk:Pubmeth
- Talk:PURA syndrome
- Talk:Pyknoachondrogenesis
- Talk:Pyloric stenosis
- Talk:Pyruvate carboxylase deficiency
- Talk:Pyruvate dehydrogenase deficiency
- Talk:Pyruvate kinase deficiency
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- Talk:Reardon-Hall-Slaney syndrome
- Category talk:Redirect-Class medical genetics articles
- Talk:Renal agenesis
- Talk:Reproductive compensation
- Talk:Retinitis pigmentosa
- Talk:Rett syndrome
- Talk:Rh deficiency syndrome
- Talk:Rheumatoid arthritis
- Talk:Ribose-5-phosphate isomerase deficiency
- Talk:Ring chromosome 20 syndrome
- Talk:Roberts syndrome
- Talk:Robertsonian translocation
- Talk:Robinow syndrome
- Talk:Rocker bottom foot
- Talk:Romano–Ward syndrome
- Talk:Varda Rotter
- Talk:Rubinstein–Taybi syndrome
- Talk:RVT-802
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- Talk:Sack–Barabas syndrome
- Talk:SACRAL syndrome
- Talk:SADDAN
- Talk:Saethre–Chotzen syndrome
- Talk:Saito–Kuba–Tsuruta syndrome
- Talk:Nadia Awni Sakati
- Talk:Salla disease
- Talk:Sandhoff disease
- Talk:Savior sibling
- Talk:Say-Field-Coldwell syndrome
- Talk:Say–Meyer syndrome
- Talk:Schimke syndrome
- Talk:Schmitt Gillenwater Kelly syndrome
- Talk:Seaver–Cassidy syndrome
- Talk:Seckel syndrome
- Talk:Jonathan Seidman
- Talk:Selenium in biology
- Talk:Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
- Talk:Sequence (medicine)
- Talk:Serrated polyposis syndrome
- Talk:Sex chromosome anomalies
- Talk:Sex linkage
- Talk:Sex selection
- Category talk:Sex selection
- Category talk:Sex selection in China
- Category talk:Sex selection in India
- Talk:Sex-chromosome dosage compensation
- Talk:Sex-determining region Y protein
- Talk:Short QT syndrome
- Talk:Short-chain acyl-coenzyme A dehydrogenase deficiency
- Talk:Sickle cell disease
- Talk:Sideroblastic anemia
- Talk:Simpson–Golabi–Behmel syndrome
- Talk:Single Specific Primer-PCR
- Talk:Single umbilical artery
- Talk:Singleton Merten syndrome
- Talk:Situs inversus
- Talk:Skin fragility-woolly hair-palmoplantar keratoderma syndrome
- Talk:Smith–Fineman–Myers syndrome
- Talk:Smith–Lemli–Opitz syndrome
- Talk:Smith–Magenis syndrome
- Talk:Smith–Martin–Dodd syndrome
- Talk:SMPD1-associated Niemann–Pick disease
- Talk:SOFT syndrome
- Talk:SonicParanoid
- Talk:Sonoda syndrome
- Talk:SPATA16
- Talk:SPG15 (disease)
- Talk:Spina bifida
- Talk:Spinal and bulbar muscular atrophy
- Talk:Spinal muscular atrophies
- Talk:Spinal muscular atrophy with lower extremity predominance 2A
- Talk:Spinocerebellar ataxia
- Talk:Spinocerebellar ataxia type 1
- Talk:Split hand split foot-nystagmus syndrome
- Talk:Spondylo-meta-epiphyseal dysplasia
- Talk:Spondylocamptodactyly
- Talk:Spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome
- Talk:Spondyloepimetaphyseal dysplasia, Strudwick type
- Talk:Spondyloepiphyseal dysplasia congenita
- Talk:Spondyloperipheral dysplasia
- Talk:Sporadic hemiplegic migraine
- Talk:SSP-PCR
- Talk:St. Helena familial genu valgum
- Category talk:Start-Class medical genetics articles
- Talk:Stickler syndrome
- Talk:Stimmler syndrome
- Talk:Stocco dos Santos syndrome
- Talk:Strømme syndrome
- Category talk:Stub-Class medical genetics articles
- Talk:Swedish mutation
- Category talk:People with Asperger syndrome
- Talk:Syndromic autism
- Talk:Systemic primary carnitine deficiency
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- Talk:T790M
- Talk:Tangier disease
- Talk:TAP deficiency syndrome
- Talk:TAR syndrome
- Talk:Taussig–Bing syndrome
- Talk:Tay–Sachs disease
- Talk:TCRB
- Category talk:Template-Class medical genetics articles
- Talk:Tetra-amelia
- Talk:Tetraamelia
- Talk:Tetrahydrobiopterin deficiency
- Talk:Tetrasomy 9p
- Talk:Tetrasomy X
- Talk:Thai symphalangism syndrome
- Talk:Thalassemia
- Talk:Thanatophoric dysplasia
- Talk:The Cancer Genome Atlas
- Talk:The Focus Foundation
- Talk:The g Factor: General Intelligence and Its Implications
- Talk:The Monarch Initiative
- Talk:Therapeutic gene modulation
- Talk:Thiamine responsive megaloblastic anemia syndrome
- Talk:Thickened earlobes-conductive deafness syndrome
- Talk:Thomsen disease
- Talk:Thoracic dysplasia-hydrocephalus syndrome
- Talk:Thrifty gene hypothesis
- Talk:Thyroid hormone resistance
- Talk:Tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome
- Talk:Tic Talk
- Talk:Timothy syndrome
- Talk:Edward Tobinick
- Category talk:Top-importance medical genetics articles
- Talk:Tourette syndrome
- Category talk:Tourette syndrome organizations
- Talk:Tourette's syndrome
- Talk:Toxicogenomics
- Talk:Transduction (genetics)
- Talk:Transgenerational epigenetic inheritance
- Talk:Transmission disequilibrium test
- Talk:Treacher Collins syndrome
- Talk:Trimethylaminuria
- Talk:Trinucleotide repeat disorder
- Talk:Trisomy 8
- Talk:Trisomy 9
- Talk:Trisomy 16
- Talk:Trisomy 18
- Talk:Trisomy 21
- Talk:Trisomy 22
- Talk:Trisomy X
- Talk:Tuberous sclerosis
- Talk:Tumor suppressor gene
- Talk:Turner syndrome
- Talk:TwinsUK
- Talk:Tyrosinemia