A novel deletion of SNURF/SNRPN exon 1 in a patient with...

European Journal of Medical Genetics 2017 / 08 Vol. 60; Iss. 8

A novel deletion of SNURF/SNRPN exon 1 in a patient with Prader-Willi-like phenotype

Cao, Yang, AlHumaidi, Susan S., Faqeih, Eissa A., Pitel, Beth A., Lundquist, Patrick, Aypar, Umut
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Volume:
60
Language:
english
Journal:
European Journal of Medical Genetics
DOI:
10.1016/j.ejmg.2017.05.003
Date:
August, 2017
File:
PDF, 1.45 MB
english, 2017
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