Prenatal diagnosis of microdeletion 16p13.11 combination with partial monosomy of 2q37.1-qter and partial trisomy of 7p15.3-pter in a fetus with bilateral ventriculomegaly, agenesis of corpus callosum, and polydactyly
2012 ◽
Vol 51
(2)
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pp. 260-265
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2005 ◽
Vol 48
(2)
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pp. 199-206
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2010 ◽
Vol 49
(3)
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pp. 320-326
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1996 ◽
Vol 16
(3)
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pp. 270-275
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Keyword(s):
2010 ◽
Vol 49
(4)
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pp. 506-512
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2006 ◽
Vol 48
(3)
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pp. 298-304
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