Absence of mutations in NR2E1 and SNX3in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes

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Bibliographic Details
Published in:BMC medical genetics 2007-07, Vol.8 (1), Article 48
Main Authors: Kumar, Ravinesh A, Everman, David B, Morgan, Chad T, Slavotinek, Anne, Schwartz, Charles E, Simpson, Elizabeth M
Format: Article
Language:English
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ISSN:1471-2350
1471-2350
DOI:10.1186/1471-2350-8-48