Microdeletion of 1p32-p31 involving NFIA in a patient with...

European Journal of Medical Genetics 2014 / 05 Vol. 57; Iss. 6

Microdeletion of 1p32-p31 involving NFIA in a patient with hypoplastic corpus callosum, ventriculomegaly, seizures and urinary tract defects

Ji, Jianling, Salamon, Noriko, Quintero-Rivera, Fabiola
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Volume:
57
Language:
english
Journal:
European Journal of Medical Genetics
DOI:
10.1016/j.ejmg.2014.03.004
Date:
May, 2014
File:
PDF, 303 KB
english, 2014
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