Novel Mutations Including Deletions of the Entire OFD1 Gene in 30 Families with Type 1 Orofaciodigital Syndrome: A Study of the Extensive Clinical Variability
Bisschoff, Izak J., Zeschnigk, Christine, Horn, Denise, Wellek, Brigitte, Rieß, Angelika, Wessels, Maja, Willems, Patrick, Jensen, Peter, Busche, Andreas, Bekkebraten, Jens, Chopra, Maya, Hove, HanneТом:
34
Мова:
english
Журнал:
Human Mutation
DOI:
10.1002/humu.22224
Date:
January, 2013
Файл:
PDF, 480 KB
english, 2013
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