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Craniofacial abnormalities and developmental delay in two families with overlapping 22q12.1 microdeletions involving the MN1 gene
Beck, Megan, Peterson, Jess F., McConnell, Juliann, McGuire, Marianne, Asato, Miya, Losee, Joseph E., Surti, Urvashi, Madan-Khetarpal, Suneeta, Rajkovic, Aleksandar, Yatsenko, Svetlana A.Volume:
167
Language:
english
Journal:
American Journal of Medical Genetics Part A
DOI:
10.1002/ajmg.a.36839
Date:
May, 2015
File:
PDF, 1.63 MB
english, 2015