Congenital heart defects in recurrent reciprocal 1q21.1 deletion and duplication syndromes: Rare association with pulmonary valve stenosis
Digilio, M. Cristina, Bernardini, Laura, Consoli, Federica, Lepri, Francesca R., Giuffrida, M. Grazia, Baban, Anwar, Surace, Cecilia, Ferese, Rosangela, Angioni, Adriano, Novelli, Antonio, Marino, BruVolume:
56
Language:
english
Journal:
European Journal of Medical Genetics
DOI:
10.1016/j.ejmg.2012.12.004
Date:
March, 2013
File:
PDF, 507 KB
english, 2013