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Results 31 - 40 of 1,198 for MS
  1. Catecholaminergic polymorphic ventricular tachycardia 
    ... JS, Bezzina CR, Bhuiyan ZA, Celiker A, Cerrone M, Dagradi F, De Ferrari GM, Etheridge SP, Fatah M, Garcia-Pavia P, Al-Ghamdi S, Hamilton RM, Al-Hassnan ZN, Horie M, Jimenez-Jaimez J, Kanter RJ, Kaski JP, Kotta ...
    https://medlineplus.gov/...ergic-polymorphic-ventricular-tachycardia - Genetics
  2. Deoxyguanosine kinase deficiency 
    ... PubMed Alberio S, Mineri R, Tiranti V, Zeviani M. Depletion of mtDNA: syndromes and genes. Mitochondrion. 2007 ... Dec 5. Citation on PubMed Brahimi N, Jambou M, Sarzi E, Serre V, Boddaert N, Romano S, ...
    https://medlineplus.gov/.../deoxyguanosine-kinase-deficiency - Genetics
  3. Gyrate atrophy of the choroid and retina 
    ... L, de Koning TJ, Poll-The BT, Duran M, Mandell R, Shih VE, Berger R, Olpin SE, ... s10545-005-0074-1. Citation on PubMed Fleury M, Barbier R, Ziegler F, Mohr M, Caron O, ...
    https://medlineplus.gov/.../gyrate-atrophy-of-the-choroid-and-retina - Genetics
  4. 1q21.1 microdeletion 
    ... T, Lalani SR, Graham B, Lee B, Shinawi M, Shen J, Kang SH, Pursley A, Lotze T, ... D, Chow E, Martell S, Tyson C, Hrynchak M, McGillivray B, Hamilton S, Marles S, Mhanni A, ...
    https://medlineplus.gov/genetics/condition/1q211-microdeletion - Genetics
  5. Ulcerative colitis 
    ... Boucher G, Lees CW, Franke A, D'Amato M, Taylor KD, Lee JC, Goyette P, Imielinski M, Latiano A, Lagace C, Scott R, Amininejad L, Bumpstead S, Baidoo L, Baldassano RN, Barclay M, Bayless TM, Brand S, Buning C, Colombel JF, ...
    https://medlineplus.gov/genetics/condition/ulcerative-colitis - Genetics
  6. Distal hereditary motor neuropathy, type II 
    ... 4; HMND4 PubMed Benquey T, Pion E, Cossee M, Krahn M, Stojkovic T, Perrin A, Cerino M, Molon A, Lia AS, Magdelaine C, Francou B, ... doi: 10.3390/genes13020318. Citation on PubMed Frasquet M, Rojas-Garcia R, Argente-Escrig H, Vazquez-Costa ...
    https://medlineplus.gov/...istal-hereditary-motor-neuropathy-type-ii - Genetics
  7. 16p11.2 duplication 
    ... I, Conus P, Ferrari C, Forzano F, Gerard M, Goin-Kochel RP, Grant E, Hunter JV, Isidor ... A, Mignot C, Mukherjee P, Owen MJ, Passeggeri M, Rooryck-Thambo C, Rosenfeld JA, Spence SJ, Steinman ...
    https://medlineplus.gov/genetics/condition/16p112-duplication - Genetics
  8. X-linked acrogigantism 
    ... A, Lodish MB, Trivellin G, Rostomyan L, Lee M, Faucz FR, Yuan B, Choong CS, Caberg JH, ... Neggers SJ, Salvatori R, Jaffrain-Rea ML, Zacharin M, Santamaria BL, Zacharieva S, Lim EM, Mantovani G, ...
    https://medlineplus.gov/genetics/condition/x-linked-acrogigantism - Genetics
  9. Frontotemporal dementia with parkinsonism-17 
    ... FRONTOTEMPORAL DEMENTIA 1; FTD1 PubMed Boeve BF, Hutton M. Refining frontotemporal dementia with parkinsonism linked to chromosome ... Epub 2012 Jul 19. Citation on PubMed Hutton M, Lendon CL, Rizzu P, Baker M, Froelich S, ...
    https://medlineplus.gov/...ntotemporal-dementia-with-parkinsonism-17 - Genetics
  10. Lamellar ichthyosis 
    ... ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 3; ARCI3 PubMed Akiyama M. ABCA12 mutations and autosomal recessive congenital ichthyosis: a ... Citation on PubMed Farasat S, Wei MH, Herman M, Liewehr DJ, Steinberg SM, Bale SJ, Fleckman P, ...
    https://medlineplus.gov/genetics/condition/lamellar-ichthyosis - Genetics
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