Phenotypic spectrum of 80 Greek patients referred as Noonan syndrome and PTPN11 mutation analysis: the value of initial clinical assessment
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S. Kitsiou-Tzeli | A. Papadopoulou | H. Fryssira | Michalis Issakidis | E. Gole | K. Kosma | A. Fretzayas | P. Nicolaidou | S. Kitsiou‐Tzeli | Evangelia Gole