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:Noninvasive prenatal testing
- Talk:Nonsyndromic deafness
- Talk:Noonan syndrome
- Talk:Noonan syndrome with multiple lentigines
- Talk:Normal People Scare Me
- Talk:Norman–Roberts syndrome
- Talk:Norrie disease
- Talk:Northern epilepsy syndrome
- Talk:Novartis Gene Therapies
- Talk:Nuclear gene
- Talk:Nuclear protein in testis gene
- Talk:Ostravik-Lindemann-Solberg syndrome
- Talk:Nuclear sexing
- Talk:Nucleic acid amplification
- Talk:Nucleic Acid Amplification
- Talk:Nucleotide salvage
- Talk:Nullisomic
- Talk:Nvidia Parabricks
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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: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:Prothrombin G20210A
- Talk:Proud syndrome
- Talk:Pseudocholinesterase deficiency
- Talk:Pseudodeficiency alleles
- Talk:Pseudohypertrophic dystrophy
- Talk:PSI (prion)
- 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