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Journal Abstract Search

216 related items for PubMed ID: 9028462

  • 1. De novo trisomy 16p.
    Carrasco Juan JL, Cigudosa JC, Otero Gómez A, Acosta Almeida MT, García Miranda JL.
    Am J Med Genet; 1997 Jan 20; 68(2):219-21. PubMed ID: 9028462
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  • 4. De novo tandem duplication of the middle segment of the long arm of chromosome 14.
    Ito M, Mutoh K, Okuno T, Mikawa H, Edagawa J, Abe T.
    Ann Genet; 1983 Jan 20; 26(2):116-9. PubMed ID: 6604486
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  • 5. 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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  • 7. 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 01; 39(2):212-5. PubMed ID: 9575279
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  • 11. Comparative genomic hybridization reveals a partial de novo trisomy 6q23-qter in an infant with congenital malformations: delineation of the phenotype.
    Erdel M, Duba HC, Verdorfer I, Lingenhel A, Geiger R, Gutenberger KH, Ludescher E, Utermann B, Utermann G.
    Hum Genet; 1997 May 01; 99(5):596-601. PubMed ID: 9150724
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  • 14. [Trisomy 5p: a report of 2 cases].
    Alvarez-Coca J, García-Alix A, Delicado A, González M, Escribá R, López Pajares I, Morena V, Peralta A.
    An Esp Pediatr; 1985 Mar 31; 22(4):288-92. PubMed ID: 4003955
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  • 16. Inverted duplication of chromosome 5p14p15.3 confirmed with in situ hybridization.
    Zenger-Hain JL, Van Dyke DL, Wiktor A, Walker H, Feldman GL.
    Am J Med Genet; 1993 Dec 01; 47(8):1198-201. PubMed ID: 8291556
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  • 18. De novo "pure" partial trisomy (6)(p22.1-->pter) in a chromosome 15 with an enlarged satellite, identified by microdissection.
    Engelen JJ, Marcelis CL, Alofs MG, Loneus WH, Pulles-Heintzberger CF, Hamers AJ.
    Am J Med Genet; 2001 Feb 15; 99(1):48-53. PubMed ID: 11170093
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  • 19. Duplication of chromosome region (16)(p11.2 --> p12.1) in a mother and daughter with mild mental retardation.
    Engelen JJ, de Die-Smulders CE, Dirckx R, Verhoeven WM, Tuinier S, Curfs LM, Hamers AJ.
    Am J Med Genet; 2002 Apr 22; 109(2):149-53. PubMed ID: 11977164
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  • 20. A father and son with mental retardation, a characteristic face, inv(12), and insertion trisomy 12p12.3-p11.2.
    Liang D, Wu L, Pan Q, Harada N, Long Z, Xia K, Yoshiura K, Dai H, Niikawa N, Cai F, Xia J.
    Am J Med Genet A; 2006 Feb 01; 140(3):238-44. PubMed ID: 16411213
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