ArticleHuman genetics2012
Spread of X-chromosome inactivation into chromosome 15 is associated with Prader-Willi syndrome phenotype in a boy with a t(X;15)(p21.1;q11.2) translocation.
Satoru Sakazume et al.PubMed ↗Publisher ↗
No numbers read from the abstract.
9 papers cite it
this papertrialcites it