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:Occipital horn syndrome
- Talk:Ocular albinism
- Talk:Ocular albinism type 1
- Talk:Oculocutaneous albinism
- Talk:Oculodentodigital dysplasia
- Talk:Oculopharyngeal muscular dystrophy
- Talk:Odontoma dysphagia syndrome
- Talk:Omenn syndrome
- Talk:Oncogene
- Talk:Ornithine aminotransferase deficiency
- Talk:Ornithine transcarbamylase deficiency
- Talk:Donald O'Rourke
- Talk:Osimertinib
- Talk:OSLAM syndrome
- Talk:Osteogenesis imperfecta
- Talk:Osteopathia striata with cranial sclerosis
- Talk:Osteoporosis-pseudoglioma syndrome
- Talk:Oto-palato-digital syndrome
- Talk:Otospondylomegaepiphyseal dysplasia
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- Talk:P.C.R.
- Talk:Pallister–Hall syndrome
- Talk:Pallister–Killian syndrome
- Talk:Palmoplantar ectodermal dysplasia
- Talk:Pancreaticobiliary maljunction
- Talk:PANO1
- Talk:Papillorenal syndrome
- Talk:Paramutation
- Talk:Paramyotonia congenita
- Category talk:Parasitic twin
- Category talk:Parasitic twinning in culture
- Talk:Partial androgen insensitivity syndrome
- Talk:Pashayan syndrome
- Talk:Patau syndrome
- Talk:Paternal mtDNA transmission
- Talk:Pattern hair loss
- Talk:PCR (disambiguation)
- Talk:PCR amplification
- Talk:PCR oil
- Talk:PCR reaction
- Talk:Pcr test
- Talk:PCR test
- Talk:PCR testing
- Talk:Pectus excavatum
- Talk:PEHO syndrome
- Talk:Pelizaeus–Merzbacher disease
- Talk:PELVIS syndrome
- Talk:Pendred syndrome
- Talk:Penetrance
- Talk:Penta X syndrome
- Talk:Pentasomy X
- Category talk:People with albinism
- Category talk:People with Crohn's disease
- Category talk:People with ulcerative colitis
- Talk:List of people with Down syndrome
- Category talk:People with genetic disorders
- Category talk:People with inflammatory bowel disease
- Category talk:People with parasitic twins
- Category talk:People with spina bifida
- Talk:Periodic paralysis
- Talk:Perlman syndrome
- Talk:Persistent Müllerian duct syndrome
- Talk:Personal genomics
- Talk:Personalized medicine
- Talk:Personalized onco-genomics
- Talk:Peters-plus syndrome
- Talk:Peutz–Jeghers syndrome
- Talk:Pfeiffer syndrome
- Talk:Pharmacogenetics
- Talk:Pharmacogenomics
- Talk:Phenylalanine hydroxylase
- Talk:Phenylketonuria
- Talk:Philadelphia chromosome
- Talk:Photic sneeze reflex
- Talk:Pierre Robin sequence
- Talk:Pioneer Fund
- Talk:Pitt–Hopkins syndrome
- Talk:Plasmodium falciparum erythrocyte membrane protein 1
- Talk:Platyspondylic lethal skeletal dysplasia
- Talk:Platyspondylic lethal skeletal dysplasia, Torrance type
- Talk:Ploidy
- 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