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Journal Abstract Search

355 related items for PubMed ID: 9138155

  • 1. Detection of a de novo duplication of 1q32-qter by fluorescence in situ hybridisation in a boy with multiple malformations: further delineation of the trisomy 1q syndrome.
    Duba HC, Erdel M, Löffler J, Bereuther L, Fischer H, Utermann B, Utermann G.
    J Med Genet; 1997 Apr; 34(4):309-13. PubMed ID: 9138155
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  • 4. De novo 1q32q44 duplication and distal 1q trisomy syndrome.
    Nowaczyk MJ, Bayani J, Freeman V, Watts J, Squire J, Xu J.
    Am J Med Genet A; 2003 Jul 15; 120A(2):229-33. PubMed ID: 12833404
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  • 7. Clinical and molecular cytogenetic characterization of two patients with partial trisomy 1q41-qter: further delineation of partial trisomy 1q syndrome.
    Emberger W, Petek E, Kroisel PM, Zierler H, Wagner K.
    Am J Med Genet; 2001 Dec 15; 104(4):312-8. PubMed ID: 11754067
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  • 8. Partial trisomy 13 in an infant with a mild phenotype: application of fluorescence in situ hybridization in cytogenetic syndromes.
    Begovic D, Hitrec V, Lasan R, Letica L, Baric I, Sarnavka V, Galic S.
    Croat Med J; 1998 Jun 15; 39(2):212-5. PubMed ID: 9575279
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  • 10. Prenatal diagnosis of partial trisomy 1q using fluorescent in situ hybridization.
    DuPont BR, Huff RW, Ridgway LE, Stratton RF, Moore CM.
    Am J Med Genet; 1994 Mar 01; 50(1):21-7. PubMed ID: 8160748
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  • 13. De novo proximal duplication of 1(q12q22) in a female infant with multiple congenital anomalies.
    Sawyer JR, Binz RL, Swanson CM, Lim C.
    Am J Med Genet A; 2007 Feb 15; 143(4):338-42. PubMed ID: 17230489
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  • 16. Distal partial trisomy 1q: report of two cases and a review of the literature.
    Utine GE, Aktas D, Alanay Y, Gücer S, Tuncbilek E, Mrasek K, Liehr T.
    Prenat Diagn; 2007 Sep 15; 27(9):865-71. PubMed ID: 17605151
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