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Journal Abstract Search

286 related items for PubMed ID: 8494030

  • 1. Trisomy 22 confirmed by fluorescent in situ hybridization.
    Stratton RF, DuPont BR, Mattern VL, Young RS, McCourt JW, Moore CM.
    Am J Med Genet; 1993 Apr 01; 46(1):109-12. PubMed ID: 8494030
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  • 3. Trisomy 22 in a liveborn infant with multiple congenital anomalies.
    McPherson E, Stetka DG.
    Am J Med Genet; 1990 May 01; 36(1):11-4. PubMed ID: 2333899
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  • 4. Terminal tandem duplication of 16p: a case with "pure" partial trisomy (16)(pter-->p13).
    Tschernigg M, Petek E, Leonhardtsberger A, Wagner K, Kroisel PM.
    Genet Couns; 2002 May 01; 13(3):303-7. PubMed ID: 12416638
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  • 5. Trisomy 20q caused by der(4) t(4;20) (q35;q13.1): report of a new patient and review of the literature.
    Plotner PL, Smith JL, Northrup H.
    Am J Med Genet; 2002 Jul 22; 111(1):71-5. PubMed ID: 12124739
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  • 6. Use of fluorescence in situ hybridization to clarify a complex chromosomal rearrangement in a child with multiple congenital anomalies.
    Spikes AS, Hegmann K, Smith JL, Shaffer LG.
    Am J Med Genet; 1995 May 22; 57(1):31-4. PubMed ID: 7645595
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  • 7. Delineation of a supernumerary marker chromosome utilizing a multimodal approach of G-banding, fluorescent in situ hybridization, confirmatory P1 artificial chromosome fluorescent in situ hybridization, and high-resolution comparative genomic hybridization.
    Mark HF, Wyandt H, Huang XL, Milunsky JM.
    Clin Genet; 2005 Aug 22; 68(2):146-51. PubMed ID: 15996211
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  • 9. Detection of a subtle rearrangement of chromosome 22 using molecular techniques.
    Biesecker LG, Rosenberg M, Dziadzio L, Ledbetter DH, Ning Y, Sarneso C, Rosenbaum K.
    Am J Med Genet; 1995 Sep 25; 58(4):389-94. PubMed ID: 8533859
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  • 10. 10p duplication characterized by fluorescence in situ hybridization.
    Wiktor A, Feldman GL, Kratkoczki P, Ditmars DM, Van Dyke DL.
    Am J Med Genet; 1994 Sep 01; 52(3):315-8. PubMed ID: 7528972
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  • 12. Brief clinical report: non-mosaic partial tetrasomy and partial trisomy 9.
    Shapiro SD, Hansen KL, Littlefield CA.
    Am J Med Genet; 1985 Feb 01; 20(2):271-6. PubMed ID: 3976720
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  • 15. Maternal origin and clinical findings in a case with trisomy 22.
    Mihçi E, Taçoy S, Yakut S, Ongun H, Keser I, Kiliçarslan B, Bağci G, Lüleci G.
    Turk J Pediatr; 2007 Feb 01; 49(3):322-6. PubMed ID: 17990591
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  • 16. A complex chromosome rearrangement with at least five breakpoints studied by fluorescence in situ hybridization.
    Gibson LH, McGrath J, Yang-Feng TL.
    Am J Med Genet; 1997 Feb 11; 68(4):417-20. PubMed ID: 9021014
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  • 18. Pure partial trisomy 7q: two new patients and review.
    Rodríguez L, López F, Paisán L, de la Red Mdel M, Ruiz AM, Blanco M, Antelo Cortizas J, Martínez-Frías ML.
    Am J Med Genet; 2002 Nov 22; 113(2):218-24. PubMed ID: 12407716
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  • 20. Familial 10p trisomy resulting from a maternal pericentric inversion.
    Kozma C, Meck JM.
    Am J Med Genet; 1994 Feb 01; 49(3):281-7. PubMed ID: 8209887
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