Bassem Bejjani

Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations

The American Journal of Human Genetics · 2009 · 342 citations

Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader-Willi syndrome

Case report · European Journal of Human Genetics · 2010 · 261 citations