Co-occurring PTPN11 and SOS1 gene mutations in Noonan syndrome does this predict a more severe phenotype?
Amanda Salem Brasil Alexsandra C Malaquias; Luciana Turolla Wanderley; Chong Ae Kim; José Eduardo Krieger; Alexander A. L Jorge; Alexandre C Pereira; Débora Romeo Bertola
Arquivos Brasileiros de Endocrinologia e Metabologia São Paulo v. 54, n. 8, p. 717-722, 2010São Paulo 2010
Localização: FM - Fac. Medicina (BCSEP 343 2010 )(Acessar)
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bcsep 344 2005
bcsep 343 2004
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