Prader-Willi syndrome and Tay-Sachs disease in association with mixed maternal uniparental isodisomy and heterodisomy 15 in a girl who also had isochromosome Xq
Zeesman, Susan, McCready, Elizabeth, Sadikovic, Bekim, Nowaczyk, Małgorzata JMVolume:
167
Language:
english
Journal:
American Journal of Medical Genetics Part A
DOI:
10.1002/ajmg.a.36790
Date:
January, 2015
File:
PDF, 445 KB
english, 2015