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Journal Abstract Search

406 related items for PubMed ID: 2705479

  • 1. New chromosome aberration: duplication of a large part of chromosome 4q and partial deletion of chromosome 1q.
    Merlob P, Kohn G, Litwin A, Nissenkorn I, Katznelson MB, Reisner SH.
    Am J Med Genet; 1989 Jan; 32(1):22-6. PubMed ID: 2705479
    [Abstract] [Full Text] [Related]

  • 2. De novo translocation involving chromosomes 1 and 4 resulting in partial duplication of 4q and partial deletion of 1p.
    Legare JM, Sekhon GS, Laxova R.
    Am J Med Genet; 1994 Nov 15; 53(3):216-21. PubMed ID: 7856655
    [Abstract] [Full Text] [Related]

  • 3. Partial duplication 4q and deletion 1p36 in monozygotic twins with discordant phenotypes.
    Angle B, Yen F, Hersh JH, Gowans G, Barch M.
    Am J Med Genet; 2002 Aug 15; 111(3):307-12. PubMed ID: 12210328
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  • 4. Familial t (4;21)(q2.4;q2.2) leading to unbalanced offspring with partial duplication of 4q and of 21q without manifestations of the Down syndrome.
    Kitsiou-Tzeli S, Hallett JJ, Atkins L, Latt SA, Holmes LB.
    Am J Med Genet; 1984 Aug 15; 18(4):725-9. PubMed ID: 6237580
    [Abstract] [Full Text] [Related]

  • 5. Translocation/duplication of 9p onto a duplicated 4q.
    Rivera H, Figuera LE, Vasquez AI.
    Genet Couns; 1992 Aug 15; 3(4):201-3. PubMed ID: 1472355
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  • 6. Child with deletion of 4q and duplication of 1q.
    Wade J, Morgan T, Allanson J.
    Am J Med Genet; 1989 Aug 15; 33(4):553-4. PubMed ID: 2596517
    [No Abstract] [Full Text] [Related]

  • 7. Double chromosome anomaly: interstitial deletion 5q and reciprocal translocation (1;11)(p22;q21).
    de Michelena MI, Villacorta J, Chávez J.
    Am J Med Genet; 1990 May 15; 36(1):29-32. PubMed ID: 2185634
    [Abstract] [Full Text] [Related]

  • 8. Clinical variability of partial duplication 1q: a clinical report and literature review.
    Rosenthal J, Abeliovich D, Carmi R.
    Am J Med Genet; 1987 Aug 15; 27(4):787-92. PubMed ID: 3122569
    [Abstract] [Full Text] [Related]

  • 9. Duplication 4q associated with chronic cholestatic changes in liver biopsy.
    Egritas O, Cavdarli B, Dalgic B, Ergun MA, Percin F, Ziegler M, Pohle B, Liehr T.
    Eur J Med Genet; 2010 Aug 15; 53(6):411-4. PubMed ID: 20826235
    [Abstract] [Full Text] [Related]

  • 10. Proximal deletion of chromosome 21 confirmed by in situ hybridization and molecular studies.
    Courtens W, Petersen MB, Noël JC, Flament-Durand J, Van Regemorter N, Delneste D, Cochaux P, Verschraegen-Spae MR, Van Roy N, Speleman F.
    Am J Med Genet; 1994 Jul 01; 51(3):260-5. PubMed ID: 8074156
    [Abstract] [Full Text] [Related]

  • 11. Partial 4q duplication due to inherited der(20), t(4;20)(q25;q13)mat.
    Sparkes RS, Francke U, Muller H, Toomey K.
    Ann Genet; 1977 Mar 01; 20(1):31-5. PubMed ID: 302670
    [Abstract] [Full Text] [Related]

  • 12. Unbalanced mosaic karyotypes with different structural abnormalities involving a common chromosome region: report of two cases.
    Pettenati MJ, Teot LA, Smith C, Hayworth R, Thomas IT, Veille JC, Rao PN.
    Am J Med Genet; 1993 Feb 01; 45(3):365-9. PubMed ID: 8434625
    [Abstract] [Full Text] [Related]

  • 13. Partial trisomy 4q due to a maternal translocation: t(4;18)(q27;q21.31).
    Van Buggenhout G, Moerman PH, Fryns JP.
    Genet Couns; 1997 Feb 01; 8(1):19-24. PubMed ID: 9101274
    [Abstract] [Full Text] [Related]

  • 14. Multiple congenital anomalies due to partial 2p13----2pter duplication resulting from an unbalanced X;2 translocation.
    Sarda P, Lefort G, Devaux P, Humeau C, Rieu D.
    Ann Genet; 1992 Feb 01; 35(2):117-20. PubMed ID: 1524409
    [Abstract] [Full Text] [Related]

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  • 16. Duplication 16q12----qter arising from 3:1 segregation in a 46,XX,t(13;16) (q12;q12) mother.
    Pérez-Castillo A, Martin-Lucas MA, Abrisqueta JA.
    Ann Genet; 1990 Feb 01; 33(2):121-3. PubMed ID: 2241087
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  • 18. An unusual clinical characterization of a male with distal partial trisomy 1q42.1 and monosomy 4q35.1 and review of the literature.
    Wang CB, Lin SP, Chen CP, Chen YJ, Lee CC.
    Genet Couns; 2006 Feb 01; 17(4):435-40. PubMed ID: 17375530
    [Abstract] [Full Text] [Related]

  • 19. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation.
    Tüysüz B, Hacihanefioglu S, Silahtaroglu A, Yilmaz S, Deviren A, Cenani A.
    Genet Couns; 2000 Feb 01; 11(4):355-61. PubMed ID: 11140413
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