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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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Novel homozygous ALX4 mutation causing frontonasal dysplasia-2 in a patient with meningoencephalocele
V A Meloni1, M Moysés-Oliveira1, M C C Melo2
1Department of Morphology and Genetics, Genetics Division, Universidade Federal de São Paulo, São Paulo, Brazil.
Clinical Genetics
|May 13, 2015
Abstract
No abstract available in PubMed .
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