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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

71 related items for PubMed ID: 11396950

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  • 4. Mapping a dominant form of multinodular goiter to chromosome Xp22.
    Capon F, Tacconelli A, Giardina E, Sciacchitano S, Bruno R, Tassi V, Trischitta V, Filetti S, Dallapiccola B, Novelli G.
    Am J Hum Genet; 2000 Oct; 67(4):1004-7. PubMed ID: 10986044
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  • 5. A novel locus for autosomal dominant nonsyndromic hearing loss (DFNA44) maps to chromosome 3q28-29.
    Modamio-Høybjør S, Moreno-Pelayo MA, Mencía A, del Castillo I, Chardenoux S, Armenta D, Lathrop M, Petit C, Moreno F.
    Hum Genet; 2003 Jan; 112(1):24-8. PubMed ID: 12483295
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  • 8. Identification of a novel locus on 2q for autosomal dominant high-grade myopia.
    Paluru PC, Nallasamy S, Devoto M, Rappaport EF, Young TL.
    Invest Ophthalmol Vis Sci; 2005 Jul; 46(7):2300-7. PubMed ID: 15980214
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  • 10. Autosomal dominant infantile gastroesophageal reflux disease: exclusion of a 13q14 locus in five well characterized families.
    Orenstein SR, Shalaby TM, Finch R, Pfuetzer RH, DeVandry S, Chensny LJ, Bannada MM, Whitcomb DC.
    Am J Gastroenterol; 2002 Nov; 97(11):2725-32. PubMed ID: 12425539
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  • 12. Genetic linkage of autosomal dominant primary open angle glaucoma to chromosome 3q in a Greek pedigree.
    Kitsos G, Eiberg H, Economou-Petersen E, Wirtz MK, Kramer PL, Aspiotis M, Tommerup N, Petersen MB, Psilas K.
    Eur J Hum Genet; 2001 Jun; 9(6):452-7. PubMed ID: 11436127
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  • 15. Localization of a novel autosomal recessive hypotrichosis locus (LAH3) to chromosome 13q14.11-q21.32.
    Wali A, Chishti M, Ayub M, Yasinzai M, Kafaitullah, Ali G, John P, Ahmad W.
    Clin Genet; 2007 Jul; 72(1):23-9. PubMed ID: 17594396
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