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Journal Abstract Search

121 related items for PubMed ID: 2793167

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  • 2. Interstitial deletion of the short arm of chromosome 20 in arteriohepatic dysplasia (Alagille syndrome).
    Zhang F, Deleuze JF, Aurias A, Dutrillaux AM, Hugon RN, Alagille D, Thomas G, Hadchouel M.
    J Pediatr; 1990 Jan; 116(1):73-7. PubMed ID: 1967307
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  • 4. Cytologically balanced t(2;20) in a two-generation family with alagille syndrome: cytogenetic and molecular studies.
    Spinner NB, Rand EB, Fortina P, Genin A, Taub R, Semeraro A, Piccoli DA.
    Am J Hum Genet; 1994 Aug; 55(2):238-43. PubMed ID: 8037203
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  • 8. 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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  • 9. Autistic disorder and chromosomal mosaicism 46,XY[123]/46,XY,del(20)(pter --> p12.2)[10].
    Sauter S, von Beust G, Burfeind P, Weise A, Starke H, Liehr T, Zoll B.
    Am J Med Genet A; 2003 Aug 01; 120A(4):533-6. PubMed ID: 12884434
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  • 10. Alagille syndrome in a family with duplication 20p11.
    Moog U, Engelen J, Albrechts J, Hoorntje T, Hendrikse F, Schrander-Stumpel C.
    Clin Dysmorphol; 1996 Oct 01; 5(4):279-88. PubMed ID: 8905191
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  • 11. FISH studies identify the i(20q-) anomaly as a der(20)del(20)(q11q13)idic(20)(p11).
    Li T, Xue Y, Wu Y, Pan J.
    Genes Chromosomes Cancer; 2006 Jun 01; 45(6):536-9. PubMed ID: 16506189
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  • 12. Intersitial deletion of 20p: new candidate region for Hirschsprung disease and autism?
    Michaelis RC, Skinner SA, Deason R, Skinner C, Moore CL, Phelan MC.
    Am J Med Genet; 1997 Aug 22; 71(3):298-304. PubMed ID: 9268100
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  • 13. Alagille syndrome and deletion of 20p.
    Anad F, Burn J, Matthews D, Cross I, Davison BC, Mueller R, Sands M, Lillington DM, Eastham E.
    J Med Genet; 1990 Dec 22; 27(12):729-37. PubMed ID: 2074558
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  • 14. Identification of a larger than 3 Mb deletion including JAG1 in an Alagille syndrome patient with a translocation t(3;20)(q13.3;p12.2).
    Oda T, Elkahloun AG, Meltzer PS, Okajima K, Sugiyama K, Wada Y, Chandrasekharappa SC.
    Hum Mutat; 2000 Jul 22; 16(1):92. PubMed ID: 10874319
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  • 18. Alagille syndrome (arteriohepatic dysplasia) and del(20)(p11.2).
    Legius E, Fryns JP, Eyskens B, Eggermont E, Desmet V, de Bethune G, Van den Berghe H.
    Am J Med Genet; 1990 Apr 22; 35(4):532-5. PubMed ID: 2333885
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