A 24.2-Mb deletion of 4q12→q21.21 characterized by array CGH in a 13½-year-old girl with short stature, mental retardation, developmental delay, hyperopia, exotropia, enamel defects, delayed tooth eruption and delayed puberty

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题名:	A 24.2-Mb deletion of 4q12→q21.21 characterized by array CGH in a 13½-year-old girl with short stature, mental retardation, developmental delay, hyperopia, exotropia, enamel defects, delayed tooth eruption and delayed puberty
作者:	Chih-Ping Chen;Shuan-Pei Lin;Yi-Ning Su;Schu-Rern Chern;Fuu-Jen Tsai;Pei-Chen Wu;Li-Feng Chen;Wayseen Wang
贡献者:	生醫所
日期:	2011-09-01
上传时间:	2015-03-16 15:40:31 (UTC+8)
關聯:	Genetic Counseling, 22(3), 255-261.
显示于类别:	[生物醫學研究所] 期刊論文

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