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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

360 related items for PubMed ID: 10512674

  • 21. A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q.
    Guilford P, Ben Arab S, Blanchard S, Levilliers J, Weissenbach J, Belkahia A, Petit C.
    Nat Genet; 1994 Jan; 6(1):24-8. PubMed ID: 8136828
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  • 22. A sensorineural progressive autosomal recessive form of isolated deafness, DFNB13, maps to chromosome 7q34-q36.
    Mustapha M, Chardenoux S, Nieder A, Salem N, Weissenbach J, el-Zir E, Loiselet J, Petit C.
    Eur J Hum Genet; 1998 Jan; 6(3):245-50. PubMed ID: 9781028
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  • 25. Homozygous CRYBB1 deletion mutation underlies autosomal recessive congenital cataract.
    Cohen D, Bar-Yosef U, Levy J, Gradstein L, Belfair N, Ofir R, Joshua S, Lifshitz T, Carmi R, Birk OS.
    Invest Ophthalmol Vis Sci; 2007 May; 48(5):2208-13. PubMed ID: 17460281
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  • 26. Linkage of pycnodysostosis to chromosome 1q21 by homozygosity mapping.
    Gelb BD, Edelson JG, Desnick RJ.
    Nat Genet; 1995 Jun; 10(2):235-7. PubMed ID: 7663521
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  • 32. Homozygosity mapping to chromosome 5p15 of a gene responsible for Hartnup disorder.
    Nozaki J, Dakeishi M, Ohura T, Inoue K, Manabe M, Wada Y, Koizumi A.
    Biochem Biophys Res Commun; 2001 Jun 08; 284(2):255-60. PubMed ID: 11394870
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  • 37. Results of penetrating keratoplasty in CHED. Congenital hereditary endothelial dystrophy.
    Sajjadi H, Javadi MA, Hemmati R, Mirdeghan A, Parvin M, Nassiri N.
    Cornea; 1995 Jan 08; 14(1):18-25. PubMed ID: 7712731
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  • 38. [Gene mapping of a nonsyndromic hearing impairmint family].
    Cheng L, Gong Y, Liu Q, Chen B, Guo C, Li J, Zhang X, Lu Y, Gao G, Zhou H, Guo Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Apr 08; 20(2):89-93. PubMed ID: 12673573
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