Works matching IS 01973851 AND DT 1997 AND VI 17 AND IP 3


Results: 13
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    Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlations.

    Published in:
    1997
    By:
    • HSU, LILLIAN Y. F.;
    • YU, MING-TSUNG;
    • NEU, RICHARD L.;
    • VAN DYKE, DANIEL L.;
    • BENN, PETER A.;
    • BRADSHAW, CHRISTY L.;
    • SHAFFER, LISA G.;
    • HIGGINS, RODNEY R.;
    • KHODR, GABRIEL S.;
    • MORTON, CYNTHIA C.;
    • WANG, HUNGSHU;
    • BROTHMAN, ARTHUR R.;
    • CHADWICK, DIANNE;
    • DISTECHE, CHRISTINE M.;
    • JENKINS, LAUREN S.;
    • KALOUSEK, DAGMAR K.;
    • PANTZAR, TAPIO J.;
    • WYATT, PHILIP;
    • Hsu, L Y;
    • Yu, M T
    Publication type:
    journal article
    4

    Monosomy X and omphalocele.

    Published in:
    1997
    By:
    • Govaerts, L C;
    • Bongers, M Y;
    • Lammens, M M;
    • Tuerlings, J H;
    • van de Kaa, C A
    Publication type:
    Case Study
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    Letter to the Editor. Monosomy X and ompalocele.

    Published in:
    Prenatal Diagnosis, 1997, v. 17, n. 3, p. 282, doi. 10.1002/(SICI)1097-0223(199703)17:3<282::AID-PD72>3.0.CO;2-G
    By:
    • Govaerts, Lutgarde C. P.;
    • Bongers, Marlies Y.;
    • Lammens, Martin M. Y.;
    • Tuerlings, Johannes H. A. M.;
    • van de Kaa, Christina A.
    Publication type:
    Article
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