Torthaí cuardaigh - Roza Ali‐Amin

Dual molecular diagnosis contributes to atypical Prader–Willi phenotype in monozygotic twins de réir Fernanda Sarquis Jehee, Valdirene T. de Oliveira, Juliana Gurgel‐Giannetti, Rafaella X. Pietra, F.V.M. Rubatino, Natália Virtude Carobin, Gabrielle S. Vianna, Mariana L. de Freitas, Karla Fernandes, Beatriz S. V. Ribeiro, Hennie T. Brüggenwirth, Roza Ali‐Amin, Janson J. White, Zeynep Coban‐Akdemir, Shalini N. Jhangiani, Richard A. Gibbs, James R. Lupski, Monica Castro Varela, Célia Priszkulnik Koiffmann, Carla Rosenberg, Claudia M.B. Carvalho