Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 12q (12q24.21→qter) and partial monosomy 6q (6q27→qter) associated with coarctation of the aorta, ventriculomegaly and thickened nuchal fold

Published 2012 View Full Article

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Keywords

Journal

GENE

Volume 516, Issue 1, Pages 138-142

Publisher

Elsevier BV

Online

2012-12-22

DOI

10.1016/j.gene.2012.12.051

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