Prenatal diagnosis and molecular cytogenetic characterization of de novo pure partial trisomy 6p associated with microcephaly, craniosynostosis and abnormal maternal serum biochemistry

Please use this identifier to cite or link to this item: http://140.112.115.32:8080/ir/handle/987654321/2563

Title:	Prenatal diagnosis and molecular cytogenetic characterization of de novo pure partial trisomy 6p associated with microcephaly, craniosynostosis and abnormal maternal serum biochemistry
Authors:	Chih-Ping Chen;Ming Cheng;Chen-Yu Chen;Schu-Rern Chern;Peih-Shan Wu;Shun-Ping Chang;Yu-Ling Kuo;Wen-Lin Chen;Chen-Wen Pan;Wayseen Wang
Contributors:	醫學系
Date:	2014-02-01
Issue Date:	2015-12-08 12:33:28 (UTC+8)
Relation:	Gene, 536(2), 425-429. doi:10.1016/j.gene.2013.12.036
Appears in Collections:	[醫學系] 期刊論文

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