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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

122 related items for PubMed ID: 9781029

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  • 3. Exclusion of BMP6 as a candidate gene for cleidocranial dysplasia.
    Innis JW, Asher JH, Liang Y, Wang A, Wilke CM, Dierick HA, Kazen-Gillespie K, Sheldon S, Glover TW, Friedman TB.
    Am J Med Genet; 1997 Aug 22; 71(3):292-7. PubMed ID: 9268099
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  • 4. Progressive pseudorheumatoid dysplasia: report of a family and review.
    el-Shanti HE, Omari HZ, Qubain HI.
    J Med Genet; 1997 Jul 22; 34(7):559-63. PubMed ID: 9222963
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  • 7. Localization of the gene for autosomal recessive congenital hereditary endothelial dystrophy (CHED2) to chromosome 20 by homozygosity mapping.
    Hand CK, Harmon DL, Kennedy SM, FitzSimon JS, Collum LM, Parfrey NA.
    Genomics; 1999 Oct 01; 61(1):1-4. PubMed ID: 10512674
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  • 9. Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia.
    Iughetti P, Alonso LG, Wilcox W, Alonso N, Passos-Bueno MR.
    Am J Med Genet; 2000 Dec 18; 95(5):482-91. PubMed ID: 11146471
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  • 10. A new betaA1-crystallin splice junction mutation in autosomal dominant cataract.
    Bateman JB, Geyer DD, Flodman P, Johannes M, Sikela J, Walter N, Moreira AT, Clancy K, Spence MA.
    Invest Ophthalmol Vis Sci; 2000 Oct 18; 41(11):3278-85. PubMed ID: 11006214
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  • 11. Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda.
    Gedeon AK, Colley A, Jamieson R, Thompson EM, Rogers J, Sillence D, Tiller GE, Mulley JC, Gécz J.
    Nat Genet; 1999 Aug 18; 22(4):400-4. PubMed ID: 10431248
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  • 14. Autosomal dominant (Beukes) premature degenerative osteoarthropathy of the hip joint unlinked to COL2A1.
    Beighton P, Cilliers HJ, Ramesar R.
    Am J Med Genet; 1994 Dec 01; 53(4):348-51. PubMed ID: 7864044
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  • 19. First genomic localization of oculo-oto-dental syndrome with linkage to chromosome 20q13.1.
    Vieira H, Gregory-Evans K, Lim N, Brookes JL, Brueton LA, Gregory-Evans CY.
    Invest Ophthalmol Vis Sci; 2002 Aug 01; 43(8):2540-5. PubMed ID: 12147582
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  • 20. [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 01; 20(2):89-93. PubMed ID: 12673573
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