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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
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 WangVolume:
50
Year:
2011
Language:
english
DOI:
10.1016/j.tjog.2011.07.014
File:
PDF, 1.11 MB
english, 2011