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Ghada M.H. Abdel-Salam, Noriko Miyake, Maha M. Eid, Mohamed S. Abdel-Hamid, Nihal A. Hassan, Ola M. Eid, Laila K. Effat, Tarek H. El-Badry, Ghada Y. El-Kamah, Mohamed El-Darouti and Naomichi Matsumoto A homozygous mutation in RNU4ATAC as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder American Journal of Medical Genetics Part A 155

Version of Record online: 11 OCT 2011 | DOI: 10.1002/ajmg.a.34299

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