Expanding the phenotype of 22q11 deletion syndrome: the MURCS association.
Uliana V, Giordano N, Caselli R, Papa FT, Ariani F, Marcocci C, Gianetti E, Martini G, Papakostas P, Rollo F, Meloni I, Mari F, Priolo M, Renieri A, Nuti R.
Uliana V, et al. Among authors: martini g.
Clin Dysmorphol. 2008 Jan;17(1):13-17. doi: 10.1097/MCD.0b013e3282ef97ee.
Clin Dysmorphol. 2008.
PMID: 18049074