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机译:Mutation Spectrum and Phenotypic Features in Noonan Syndrome with PTPN11 Mutations: Definition of Two Novel Mutations
Ege Univ, Sch Med, Dept Pediat, Div Genet, TR-35100 Izmir, Turkey;
Ege Univ, Sch Med, Dept Med Genet, Izmir, Turkey;
Dr Behcet Uz Childrens Hosp, Dept Med Genet, Izmir, TurkeyEge Univ, Sch Med, Dept Pediat, Div Endocrinol, Izmir, TurkeyAnkara Univ, Sch Med, Dept Genet, Ankara, Turkey;
Noonan syndrome; Rasopathy; PTPN11; Pulmonary stenosis; Short stature;