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

CMUR > College of Chinese Medicine > School of Chinese Medicine > Journal articles > Item 310903500/46689

Please use this identifier to cite or link to this item: http://ir.cmu.edu.tw/ir/handle/310903500/46689

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(Chih-Ping Chen)*;(Yi-Ning Su);(Fang-Yu Hung);(Schu-Rern Chern);(Jun-Wei Su);(Wayseen Wang)
Contributors:	中醫學院中醫學系學士班中醫內科學科;中國附醫醫學研究部
Keywords:	COL1A2;mutation;deletion;osteogenesis imperfecta type II
Date:	2012-06
Issue Date:	2012-10-17 16:46:33 (UTC+8)
Relation:	Taiwanese Journal of Obstetrics & Gynecology 51(2):312-314
Appears in Collections:	[School of Chinese Medicine] Journal articles

Files in This Item:

File	Description	Size	Format
AA-BA00_20120720101805.doc		29Kb	Microsoft Word	271	View/Open