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Autor:
Stephen Nowicki, Randi J Hagerman, Michele Y. Ono, Jessica A Ferranti, Beth L. Goodlin-Jones, Flora Tassone, Marie Francoise Croquette
Publikováno v:
Journal of Developmental & Behavioral Pediatrics. 28:133-138
The Prader-Willi phenotype (PWP) of fragile X syndrome (FXS) is associated with obesity and hyperphagia similar to Prader-Willi syndrome (PWS), but without cytogenetic or methylation abnormalities at 15q11-13. Thirteen cases of PWP and FXS are report