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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

89 related items for PubMed ID: 17658607

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  • 6. Founder mutation causing infantile GM1-gangliosidosis in the Gypsy population.
    Sinigerska I, Chandler D, Vaghjiani V, Hassanova I, Gooding R, Morrone A, Kremensky I, Kalaydjieva L.
    Mol Genet Metab; 2006 May; 88(1):93-5. PubMed ID: 16466959
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  • 7. Familial CD8 deficiency due to a mutation in the CD8 alpha gene.
    de la Calle-Martin O, Hernandez M, Ordi J, Casamitjana N, Arostegui JI, Caragol I, Ferrando M, Labrador M, Rodriguez-Sanchez JL, Espanol T.
    J Clin Invest; 2001 Jul; 108(1):117-23. PubMed ID: 11435463
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  • 8. MYOC gene mutations in Spanish patients with autosomal dominant primary open-angle glaucoma: a founder effect in southeast Spain.
    Campos-Mollo E, Sánchez-Sánchez F, López-Garrido MP, López-Sánchez E, López-Martínez F, Escribano J.
    Mol Vis; 2007 Sep 13; 13():1666-73. PubMed ID: 17893668
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  • 13. Novel HMBS founder mutation and significant intronic polymorphism in Spanish patients with acute intermittent porphyria.
    Guillén-Navarro E, Carbonell P, Glover G, Sánchez-Solís M, Fernández-Barreiro A.
    Ann Hum Genet; 2004 Sep 13; 68(Pt 5):509-14. PubMed ID: 15469427
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  • 14. Gene mapping in Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24.
    Kalaydjieva L, Hallmayer J, Chandler D, Savov A, Nikolova A, Angelicheva D, King RH, Ishpekova B, Honeyman K, Calafell F, Shmarov A, Petrova J, Turnev I, Hristova A, Moskov M, Stancheva S, Petkova I, Bittles AH, Georgieva V, Middleton L, Thomas PK.
    Nat Genet; 1996 Oct 13; 14(2):214-7. PubMed ID: 8841199
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  • 18. Recurrent Respiratory Infections Revealing CD8α Deficiency.
    Dumontet E, Osman J, Guillemont-Lambert N, Cros G, Moshous D, Picard C.
    J Clin Immunol; 2015 Nov 13; 35(8):692-5. PubMed ID: 26563160
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