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Journal Abstract Search

111 related items for PubMed ID: 7789956

  • 21.
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  • 22. Segregation analysis of Alagille syndrome.
    Dhorne-Pollet S, Deleuze JF, Hadchouel M, Bonaïti-Pellié C.
    J Med Genet; 1994 Jun; 31(6):453-7. PubMed ID: 8071971
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  • 23. Confirmation of linkage of Duane's syndrome and refinement of the disease locus to an 8.8-cM interval on chromosome 2q31.
    Evans JC, Frayling TM, Ellard S, Gutowski NJ.
    Hum Genet; 2000 Jun; 106(6):636-8. PubMed ID: 10942112
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  • 24. A 8.26Mb deletion in 6q16 and a 4.95Mb deletion in 20p12 including JAG1 and BMP2 in a patient with Alagille syndrome and Wolff-Parkinson-White syndrome.
    Le Gloan L, Pichon O, Isidor B, Boceno M, Rival JM, David A, Le Caignec C.
    Eur J Med Genet; 2008 Jun; 51(6):651-7. PubMed ID: 18775522
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  • 26. A locus for autosomal dominant anterior polar cataract on chromosome 17p.
    Berry V, Ionides AC, Moore AT, Plant C, Bhattacharya SS, Shiels A.
    Hum Mol Genet; 1996 Mar; 5(3):415-9. PubMed ID: 8852669
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  • 27. Autosomal dominant gnathodiaphyseal dysplasia maps to chromosome 11p14.3-15.1.
    Tsutsumi S, Kamata N, Maruoka Y, Ando M, Tezuka O, Enomoto S, Omura K, Nagayama M, Kudo E, Moritani M, Yamaoka T, Itakura M.
    J Bone Miner Res; 2003 Mar; 18(3):413-8. PubMed ID: 12619924
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  • 30. Isolated familial somatotropinomas: establishment of linkage to chromosome 11q13.1-11q13.3 and evidence for a potential second locus at chromosome 2p16-12.
    Gadelha MR, Une KN, Rohde K, Vaisman M, Kineman RD, Frohman LA.
    J Clin Endocrinol Metab; 2000 Feb; 85(2):707-14. PubMed ID: 10690880
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  • 34. Molecular and cytogenetic analysis of an interstitial 20p deletion associated with syndromic intrahepatic ductular hypoplasia (Alagille syndrome).
    Schnittger S, Höfers C, Heidemann P, Beermann F, Hansmann I.
    Hum Genet; 1989 Oct; 83(3):239-44. PubMed ID: 2793167
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  • 38. Jagged1 mutations in patients ascertained with isolated congenital heart defects.
    Krantz ID, Smith R, Colliton RP, Tinkel H, Zackai EH, Piccoli DA, Goldmuntz E, Spinner NB.
    Am J Med Genet; 1999 May 07; 84(1):56-60. PubMed ID: 10213047
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  • 39. Evidence for linkage of restless legs syndrome to chromosome 9p: are there two distinct loci?
    Lohmann-Hedrich K, Neumann A, Kleensang A, Lohnau T, Muhle H, Djarmati A, König IR, Pramstaller PP, Schwinger E, Kramer PL, Ziegler A, Stephani U, Klein C.
    Neurology; 2008 Feb 26; 70(9):686-94. PubMed ID: 18032746
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  • 40.
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