ASIA unversity:Item 310904400/64313
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    Please use this identifier to cite or link to this item: http://asiair.asia.edu.tw/ir/handle/310904400/64313


    Title: Chromosome 18p deletion syndrome presenting holoprosencephaly and premaxillary agenesis: prenatal diagnosis and aCGH characterization using uncultured amniocytes
    Authors: 陳持平;Chen, Chih-Ping;Hua, Jian-Pei;Huang, Jian-Pei;Chen, Yi-Yung;Chen, Yi-Yung;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Pan, Chen-Wen;Pan, Chen-Wen;Wang, Wayseen;Wang, Wayseen
    Contributors: 生物科技學系
    Keywords: 18p deletion syndrome;Holoprosencephaly;Prenatal diagnosis;TGIF
    Date: 201309
    Issue Date: 2013-10-29 17:36:24 (UTC+8)
    Abstract: We present prenatal diagnosis of a de novo distal 18p deletion involving 14.06Mb at 18p11.32-p11.21 by aCGH using uncultured amniocytes in a pregnancy with fetal holoprosencephaly and premaxillary agenesis. QF-PCR analysis showed that distal 18p deletion was from maternal origin. Metaphase FISH analysis confirmed haploinsufficiency of TGIF. We discuss the functions of the genes that are deleted within this region. The present case shows the usefulness of applying aCGH on uncultured amniocytes for rapid aneuploidy diagnosis in cases with prenatally detected fetal structural abnormalities.
    Relation: GENE, 527(2):636-41.
    Appears in Collections:[Department of Biotechnology] Journal Article

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