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Journal Abstract Search

115 related items for PubMed ID: 9447751

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  • 4. Localization of Alagille syndrome to 20p11.2-p12 by linkage analysis of a three-generation family.
    Hol FA, Hamel BC, Geurds MP, Hansmann I, Nabben FA, Daniëls O, Mariman EC.
    Hum Genet; 1995 Jun; 95(6):687-90. PubMed ID: 7789956
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  • 5. Molecular analysis of 24 Alagille syndrome families identifies a single submicroscopic deletion and further localizes the Alagille region within 20p12.
    Rand EB, Spinner NB, Piccoli DA, Whitington PF, Taub R.
    Am J Hum Genet; 1995 Nov; 57(5):1068-73. PubMed ID: 7485156
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  • 6. Construction of an integrated physical and gene map of human chromosome 20p12 providing candidate genes for Alagille syndrome.
    Pollet N, Boccaccio C, Dhorne-Pollet S, Driancourt C, Raynaud N, Auffray C, Hadchouel M, Meunier-Rotival M.
    Genomics; 1997 Jun 15; 42(3):489-98. PubMed ID: 9205123
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  • 12. Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1.
    Li L, Krantz ID, Deng Y, Genin A, Banta AB, Collins CC, Qi M, Trask BJ, Kuo WL, Cochran J, Costa T, Pierpont ME, Rand EB, Piccoli DA, Hood L, Spinner NB.
    Nat Genet; 1997 Jul 15; 16(3):243-51. PubMed ID: 9207788
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  • 14. Deletions of 20p12 in Alagille syndrome: frequency and molecular characterization.
    Krantz ID, Rand EB, Genin A, Hunt P, Jones M, Louis AA, Graham JM, Bhatt S, Piccoli DA, Spinner NB.
    Am J Med Genet; 1997 May 02; 70(1):80-6. PubMed ID: 9129746
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  • 16. SNP array mapping of chromosome 20p deletions: genotypes, phenotypes, and copy number variation.
    Kamath BM, Thiel BD, Gai X, Conlin LK, Munoz PS, Glessner J, Clark D, Warthen DM, Shaikh TH, Mihci E, Piccoli DA, Grant SF, Hakonarson H, Krantz ID, Spinner NB.
    Hum Mutat; 2009 Mar 02; 30(3):371-8. PubMed ID: 19058200
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  • 19. Deleted chromosome 20 from a patient with Alagille syndrome isolated in a cell hybrid through leucine transport selection: study of three candidate genes.
    Deleuze JF, Dhorne S, Hazan J, Borghi E, Raynaud N, Pollet N, Meunier-Rotival M, Deschatrette J, Alagille D, Hadchouel M.
    Mamm Genome; 1994 Nov 02; 5(11):663-9. PubMed ID: 7873876
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