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    Please use this identifier to cite or link to this item: http://asiair.asia.edu.tw/ir/handle/310904400/16885


    Title: Identification of a COL1A2 mutation with a deletion spanning coding and intronic sequence in exon 19 and intron 19 in a fetus with osteogenesis imperfecta type II
    Authors: 陳持平;Chen, Chih-Ping
    Contributors: 生物科技學系
    Date: 2012-06
    Issue Date: 2012-11-23 09:18:04 (UTC+0)
    Relation: Taiwanese Journal of Obstetrics & Gynecology
    Appears in Collections:[生物科技學系] 期刊論文

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