Osteogenesis imperfecta type I: second-trimester diagnosis and incidental identification of a dominant COL1A1 deletion mutation in the asymptomatic father

Please use this identifier to cite or link to this item: http://140.112.115.32:8080/ir/handle/987654321/1375

Title:	Osteogenesis imperfecta type I: second-trimester diagnosis and incidental identification of a dominant COL1A1 deletion mutation in the asymptomatic father
Authors:	Chih-Ping Chen;Yi-Ning Su;Tung-Yao Chang;Schu-Rern Chern;Chen-Yu Chen;Jun-Wei Su;Wayseen Wang
Contributors:	生醫所
Date:	2012-06-01
Issue Date:	2015-03-16 15:43:10 (UTC+8)
Relation:	Taiwanese Journal of Obstetrics and Gynecology 51，276-279
Appears in Collections:	[生物醫學研究所] 期刊論文

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