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

Please use this identifier to cite or link to this item: http://140.112.115.32:8080/ir/handle/987654321/1180

Title:	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
Authors:	Chih-Ping Chen;Shuan-Pei Lin;Yi-Ning Su;Schu-Rern Chern;Fuu-Jen Tsai;Pei-Chen Wu;Li-Feng Chen;Wayseen Wang
Contributors:	生醫所
Date:	2011-09-01
Issue Date:	2015-03-16 15:40:31 (UTC+8)
Relation:	Genetic Counseling, 22(3), 255-261.
Appears in Collections:	[Institute of Biomedical Sciences] Journal papers

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