Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia and intrauterine growth restriction

Please use this identifier to cite or link to this item: http://140.112.115.32:8080/ir/handle/987654321/1229

Title:	Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia and intrauterine growth restriction
Authors:	Chih-Ping Chen;Yi-Ning Su;Yi-Yung Chen;Schu-Rern Chern;Yu-Peng Liu;Pei-Chen Wu;Chen-Chi Lee;Yu-Ting Chen;Wayseen Wang
Contributors:	生醫所
Date:	2011-09-01
Issue Date:	2015-03-16 15:40:51 (UTC+8)
Relation:	Taiwanese Journal of Obstetrics and Gynecology 50，345-352
Appears in Collections:	[生物醫學研究所] 期刊論文

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