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

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题名:	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
作者:	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
贡献者:	生醫所
日期:	2011-09-01
上传时间:	2015-03-16 15:40:51 (UTC+8)
關聯:	Taiwanese Journal of Obstetrics and Gynecology 50，345-352
显示于类别:	[生物醫學研究所] 期刊論文

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