Change in prevalence of congenital defects in children with Prader-Willi syndrome
Torrado, M, Foncuberta, M E, Perez, M F de Castro, Gravina, L P, Araoz, H V, Baialardo, E, Chertkoff, L P
Published in Pediatrics (Evanston) (01.02.2013)
Published in Pediatrics (Evanston) (01.02.2013)
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SÍNDROME DE NOONAN CON CABELLO ANÁGENO CON VARIANTES EN PPP1CB: PRIMER CASO FAMILIAR REPORTADO
Chinton, J, Huckstadt, V, Bonetto, M, Gravina, L P, Obregon, M G
Published in BAG. Journal of basic and applied genetics (01.09.2020)
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Published in BAG. Journal of basic and applied genetics (01.09.2020)
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