A case of Beckwith-Wiedemann syndrome caused by a cryptic 11p15 deletion encompassing the centromeric imprinted domain of the BWS locus
Zollino, M., Orteschi, D., Marangi, G., De Crescenzo, A., Pecile, V., Riccio, A., Neri, G.Volume:
47
Language:
english
Journal:
Journal of Medical Genetics
DOI:
10.1136/jmg.2009.071142
Date:
June, 2010
File:
PDF, 424 KB
english, 2010