Dual molecular diagnosis contributes to atypical Prader–Willi phenotype in monozygotic twins
Fernanda S Jehee Valdirene T. de Oliveira; Juliana Gurgel Giannetti; Rafaella X Pietra; Fernando V. M Rubatino; Natália V Carobin; Gabrielle S Vianna; Mariana L. de Freitas; Karla S Fernandes; Beatriz S. V Ribeiro; Hennie T Brüggenwirth; Roza Ali-Amin; Janson J White; Zeynep C Akdemir; Shalini N Jhangiani; Richard A Gibbs; James R Lupski; Monica C Varela; Celia Priszkulnik Koiffmann; Carla Rosenberg; Cláudia M. B Carvalho; Baylor-Hopkins Center for Mendelian Genomics
American Journal of Medical Genetics. Part A Hoboken online, p. 1-5, June 2017
Hoboken 2017
Item não circula. Consulte sua biblioteca.(Acessar)