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
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| Description | scientific article published on September 2011 |
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author: Chih-Ping Chen Schu-Rern Chern Wayseen Wang Chen-Chi Lee |
| Publication date | September 1, 2011 |
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