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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

236 related items for PubMed ID: 1524408

  • 21.
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  • 22. Evidence for involvement of a Robertsonian translocation 13 chromosome in formation of a ring chromosome 13.
    Stetten G, Tuck-Muller CM, Blakemore KJ, Wong C, Kazazian HH, Antonarakis SE.
    Mol Biol Med; 1990 Dec; 7(6):479-84. PubMed ID: 2077349
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  • 23.
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  • 24. Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
    Chen CP, Chern SR, Wang W, Lee CC, Chen WL, Chen LF, Chang TY, Tzen CY.
    Prenat Diagn; 2001 May; 21(5):346-50. PubMed ID: 11360273
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  • 26. [Partial trisomy of chromosome 7 due to balanced chromosome translocation in the father].
    Stumpner P.
    Geburtshilfe Frauenheilkd; 1989 Dec; 49(12):1090-2. PubMed ID: 2693190
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  • 27. Atypical Down syndrome phenotype in a girl with 21;21 translocation trisomy.
    Tuysuz B, Yavuz A, Ozdil M, Caferler J, Ozon H.
    Genet Couns; 2010 Dec; 21(1):61-7. PubMed ID: 20420031
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  • 28. Trisomy first, translocation second, uniparental disomy and partial trisomy third: a new mechanism for complex chromosomal aneuploidy.
    Schinzel A, Kotzot D, Brecevic L, Robinson WP, Dutly F, Dauwerse H, Binkert F, Baumer A, Ausserer B.
    Eur J Hum Genet; 1997 Dec; 5(5):308-14. PubMed ID: 9412788
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  • 29. Recurrent proximal 18p monosomy and 18q trisomy in a family with a maternal pericentric inversion of chromosome 18.
    Prabhakara K, Wyandt HE, Huang XL, Prasad KS, Ramadevi AR.
    Ann Genet; 2004 Dec; 47(3):297-303. PubMed ID: 15337476
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  • 32. Trisomy 9: review and report of two new cases.
    Arnold GL, Kirby RS, Stern TP, Sawyer JR.
    Am J Med Genet; 1995 Apr 10; 56(3):252-7. PubMed ID: 7778584
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  • 33.
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  • 34. Trisomy 12/monosomy X/normal female mosaicism: prenatal detection and confirmation in a liveborn.
    Spiro R, Rita D, Jazmines L, Jones C, Booth CW.
    Prenat Diagn; 1996 Aug 10; 16(8):734-40. PubMed ID: 8878284
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  • 39. Centromeric DNA break in a 10;16 reciprocal translocation associated with trisomy 16 confined placental mosaicism and maternal uniparental disomy for chromosome 16.
    Wang JC, Mamunes P, Kou SY, Schmidt J, Mao R, Hsu WT.
    Am J Med Genet; 1998 Dec 04; 80(4):418-22. PubMed ID: 9856575
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  • 40. Iniencephaly and chromosome mosaicism: a report of two cases.
    Halder A, Agarwal S, Pandey A.
    Congenit Anom (Kyoto); 2005 Sep 04; 45(3):102-5. PubMed ID: 16131369
    [Abstract] [Full Text] [Related]

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