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Journal Abstract Search

190 related items for PubMed ID: 8456834

  • 1. Duplication 9q34-->qter identified by chromosome painting.
    Spinner NB, Lucas JN, Poggensee M, Jacquette M, Schneider A.
    Am J Med Genet; 1993 Mar 01; 45(5):609-13. PubMed ID: 8456834
    [Abstract] [Full Text] [Related]

  • 2. Partial tetrasomy with triplication of chromosome (5) (p14-p15.33) in a patient with severe multiple congenital anomalies.
    Harrison KJ, Teshima IE, Silver MM, Jay V, Unger S, Robinson WP, James A, Levin A, Chitayat D.
    Am J Med Genet; 1998 Sep 01; 79(2):103-7. PubMed ID: 9741467
    [Abstract] [Full Text] [Related]

  • 3. Characterization of a duplication in the terminal band of 4p by molecular cytogenetics.
    Wyandt HE, Milunsky J, Lerner T, Gusella JF, Hou A, MacDonald M, Adekunle S, Milunsky A.
    Am J Med Genet; 1993 Apr 01; 46(1):72-6. PubMed ID: 7684190
    [Abstract] [Full Text] [Related]

  • 4. M-banding characterization of a 16p11.2p13.1 tandem duplication in a child with autism, neurodevelopmental delay and dysmorphism.
    Behjati F, Shafaghati Y, Firouzabadi SG, Kahrizi K, Bagherizadeh I, Najmabadi H, Bint S, Ogilvie C.
    Eur J Med Genet; 2008 Apr 01; 51(6):608-14. PubMed ID: 18674645
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  • 5. Molecular and cytogenetic characterization of 9p- abnormalities.
    Teebi AS, Gibson L, McGrath J, Meyn MS, Breg WR, Yang-Feng TL.
    Am J Med Genet; 1993 May 15; 46(3):288-92. PubMed ID: 8488873
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. Mosaic dup (9p) diagnosed by fluorescence in situ hybridization (FISH).
    Petty EM, Gibson LH, Breg WR, Burns JP, Yang-Feng TL.
    Am J Med Genet; 1993 Mar 15; 45(6):770-3. PubMed ID: 8456860
    [Abstract] [Full Text] [Related]

  • 8. Boy with an interstitial 1q (q31q41) duplication confirmed by fluorescent in situ hybridisation.
    Sillén A, Wadelius C, Annerén G.
    Am J Med Genet; 1998 Nov 02; 80(2):163-8. PubMed ID: 9805135
    [Abstract] [Full Text] [Related]

  • 9. Cytogenetic and molecular analysis in trisomy 12p.
    Allen TL, Brothman AR, Carey JC, Chance PF.
    Am J Med Genet; 1996 May 03; 63(1):250-6. PubMed ID: 8723118
    [Abstract] [Full Text] [Related]

  • 10. Recurrent duplication of Xq27-qter in hematological malignancies revealed by multicolor fluorescence in situ hybridization and multicolor banding.
    MacKinnon RN, Zordan A, Campbell LJ.
    Cancer Genet Cytogenet; 2005 Sep 03; 161(2):125-9. PubMed ID: 16102582
    [Abstract] [Full Text] [Related]

  • 11. Confirmation of proximal 1q duplication using fluorescence in situ hybridization.
    Chen H, Kusyk CJ, Tuck-Muller CM, Martinez JE, Dorand RD, Wertelecki W.
    Am J Med Genet; 1994 Mar 01; 50(1):28-31. PubMed ID: 8160749
    [Abstract] [Full Text] [Related]

  • 12. Complex familial rearrangement of chromosome 9p24.3 detected by FISH.
    Repetto GM, Wagstaff J, Korf BR, Knoll JH.
    Am J Med Genet; 1998 Apr 01; 76(4):306-9. PubMed ID: 9545094
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  • 14. Trisomy chromosome (22)(q13.1-qter) as a result of paternal inversion (22)(p11q13.1) proved using region-specific FISH probes.
    Hou JW.
    Chang Gung Med J; 2005 Sep 01; 28(9):657-61. PubMed ID: 16323558
    [Abstract] [Full Text] [Related]

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  • 16. Complex chromosome rearrangements and congenital anomalies.
    Kousseff BG, Nichols P, Essig YP, Miller K, Weiss A, Tedesco TA.
    Am J Med Genet; 1987 Apr 01; 26(4):771-82. PubMed ID: 3591822
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  • 19. Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization.
    Blennow E, Nielsen KB, Telenius H, Carter NP, Kristoffersson U, Holmberg E, Gillberg C, Nordenskjöld M.
    Am J Med Genet; 1995 Jan 02; 55(1):85-94. PubMed ID: 7702104
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  • 20. 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 02; 39(2):212-5. PubMed ID: 9575279
    [Abstract] [Full Text] [Related]

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