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Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype.

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Bibliographic Details
Title: Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype.
Authors: D'Amours, G1,2,3, Kibar, Z2, Mathonnet, G1, Fetni, R2,3,4,5, Tihy, F1,2,3,5, Désilets, V1,3,6, Nizard, S1,3,6, Michaud, JL1,2,3,6, Lemyre, E1,2,3,6
Source: Clinical Genetics. Feb2012, Vol. 81 Issue 2, p128-141. 14p. 1 Diagram, 3 Charts, 1 Graph.
Database: Academic Search Ultimate
Description
ISSN:00099163
DOI:10.1111/j.1399-0004.2011.01687.x