Expanding the phenotype of 22q13.3 deletion: report of a case detected prenatally.

Academic Article

Publication Date:

2008

Iris type:

1.1 Articolo in rivista

Keywords:

"DIAGNOSI PRENATALE"; "DELEZIONI CRIPTICHE"; "CROMOSOMA 22"

List of contributors:

Maitz, S; Gentilin, B; Colli, Am; Rizzuti, T; Brandolisio, E; Vetro, Annalisa; Zuffardi, Orsetta; Guerneri, S; Lalatta, F.

Authors of the University:

ZUFFARDI ORSETTA

Handle:

https://iris.unipv.it/handle/11571/119150

Published in:

PRENATAL DIAGNOSIS

Journal