Ara
Toplam kayıt 489, listelenen: 321-330
Neuromyelitis optica spectrum disorders: The evaluation of 66 patients followed by Istanbul Bilim University, Department of Neurology
(LIPPINCOTT WILLIAMS & WILKINS, 2019)
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Constitutive mismatch repair defect syndrome: New insights from whole exome sequencing data and functional studies
(ELSEVIER SCIENCE BV, 2016)
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PELVIC LYMPH NODE DISSECTION DURING ROBOT ASSISTED RADICAL PROSTATECTOMY: COMPARISION OF PREOPERATIVE AND POSTOPERATIVE DATA
(MARY ANN LIEBERT INC, 2011)
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Is the Glu298Asp polymorphism of Endothelial Nitric Oxide Synthesis Increase the Risk of Stent Thrombosis ?
(ELSEVIER SCIENCE INC, 2013)
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XRCC3 GENE POLYMORPHISM IN BLADDER CANCER
(INT INST ANTICANCER RESEARCH, 2008)
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Mutation analysis of Phospholipase C Zeta (PLC?) in patients with low fertilisation rate
(OXFORD UNIV PRESS, 2014)
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Severe Walker Warburg syndrome associated with new mutation in ISPD gene identified with whole exome sequencing
(PERGAMON-ELSEVIER SCIENCE LTD, 2016)
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