Yazar "Hancer, V. S." için WoS İndeksli Yayınlar Koleksiyonu listeleme
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MPL W515 K MUTATION IN A PEDIATRIC CASE OF ESSENTIAL THROMBOCYTHEMIA PRESENTING WITH BUDD-CHIARI SYNDROME
Tokgoz, H.; Caliskan, U.; Kucukkaya, R.; Hancer, V. S. (PERGAMON-ELSEVIER SCIENCE LTD, 2016)… -
TET2 MUTATIONS IN ESSENTIAL THROMBOCYTHEMIA AND PRIMARY MYELOFIBROSIS
Turan, C.; Guvenc, S.; Hancer, V. S.; Hindilerden, F.; Arat, M.; Kucukkaya, R. (FERRATA STORTI FOUNDATION, 2015)… -
TWO NOVEL CALRETICULIN MUTATIONS IN A TURKISH PATIENT WITH PRIMARY MYELOFIBROSIS: C.1116DELA AND C.1120A > C
Guvenc, S.; Hancer, V. S.; Uslu, N.; Arat, M.; Kucukkaya, R. (FERRATA STORTI FOUNDATION, 2015)…