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:Moebius syndrome
- Category talk:Molecular biologists by nationality
- Talk:Molecular biology
- Talk:Molecular Biology
- Category talk:Molecular genetics
- Talk:Molecular risk assessment
- Talk:Molecular Xeroxing
- Talk:Molybdenum cofactor deficiency
- Talk:MOMO syndrome
- Talk:Mongolian idiocy
- Talk:Monogenic obesity
- Talk:Moonrise (Wolfson book)
- Talk:MORM syndrome
- Talk:D. Holmes Morton
- Talk:Mosaic loss of chromosome Y
- Talk:Roxana Moslehi
- Talk:Mouse models of Down syndrome
- Talk:MPI-CDG
- Talk:Mucolipidosis
- Talk:Mucopolysaccharidosis
- Talk:Mulibrey nanism
- Talk:Multifactorial disease
- Talk:Multifocal stenosing ulceration of the small intestine
- Talk:Multiple congenital anomalies-hypotonia-seizures syndrome
- Talk:Multiple endocrine neoplasia type 1
- Talk:Multiple endocrine neoplasia type 2
- Talk:Multiple sulfatase deficiency
- Talk:Muscular dystrophy
- Talk:Muscular dystrophy - Duchenne type
- Talk:Muscular Dystrophy Association
- Talk:Muscular dystrophy Duchenne type
- Category talk:Muscular dystrophy organizations
- Talk:Muscular dystrophy, duchenne
- Talk:Muscular dystrophy, Duchenne
- Talk:Mutational meltdown
- Talk:MUTYH-associated polyposis
- Talk:Myelokathexis
- Talk:Myeloperoxidase deficiency
- Talk:Myopathy
- Talk:Myopathy, X-linked, with excessive autophagy
- Talk:Myotonia congenita
- Talk:Myotonic dystrophy
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- Talk:N-Acetylglutamate synthase deficiency
- Category talk:NA-Class medical genetics articles
- Category talk:NA-importance medical genetics articles
- Talk:Nail–patella syndrome
- Talk:Emil Najman
- Talk:Nance–Horan syndrome
- Talk:National Bleeding Disorders Foundation
- Talk:National Society of Genetic Counselors
- Talk:NcRNA therapy
- Talk:Nemaline myopathy
- Talk:Neonatal adrenoleukodystrophy
- Talk:Neonatal hemochromatosis
- Talk:Neonatal teeth
- Talk:Neotenic complex syndrome
- Talk:Neurofibromatosis
- Talk:Neurofibromatosis type I
- Talk:Neurofibromatosis type II
- Talk:Neuropathy, ataxia, and retinitis pigmentosa
- Talk:Niemann–Pick disease
- Talk:Niemann–Pick disease type C
- Talk:Nijmegen breakage syndrome
- 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: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