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
2011 ◽
Vol 50
(3)
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pp. 345-352
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2015 ◽
Vol 54
(6)
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pp. 797-798
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2010 ◽
Vol 49
(4)
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pp. 506-512
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2010 ◽
Vol 2010
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pp. 38-39
2013 ◽
Vol 52
(2)
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pp. 278-284
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2019 ◽
Vol 58
(1)
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pp. 139-144