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Epilepsy Research|May 20, 2015
A clinical variant in SCN1A inherited from a mosaic father cosegregates with a novel variant to cause Dravet syndrome in a consanguineous familyFeyza N Tuncer, Zeliha Gormez, Mustafa Calik, et al.Molecular Genetics & Genomic Medicine|August 24, 2023
A new line method; A direct test in spinal muscular atrophy screening for DBSAyhan Kubar, Sehime Gülsüm Temel, Serdar Beken, et al.Clinical Neurology and Neurosurgery|January 24, 2017
Clinical and genetic features of PKAN patients in a tertiary centre in TurkeyNihan Hande Akcakaya, Sibel Ugur Iseri, Birdal Bilir, et al.Expert Review of Hematology|September 5, 2020
Copy-number variations in adult patients with chronic immune thrombocytopeniaEmrah Yucesan, Ozden Hatirnaz Ng, Fevzi Firat Yalniz, et al.Journal of Human Genetics|June 12, 2021
The rare rs769301934 variant in NHLRC1 is a common cause of Lafora disease in TurkeyGaren Haryanyan, Ozkan Ozdemir, Kemal Tutkavul, et al.Plos One|December 6, 2021
Mutational landscape of SARS-CoV-2 genome in Turkey and impact of mutations on spike protein structureOzden Hatirnaz Ng, Sezer Akyoney, Ilayda Sahin, et al.Leukemia Research|June 23, 2019
Prognostic gene alterations and clonal changes in childhood B-ALLYucel Erbilgin, Sinem Firtina, Sevcan Mercan, et al.Tumori|June 9, 2012
SET oncogene is upregulated in pediatric acute lymphoblastic leukemiaSema Sirma Ekmekci, Cumhur G Ekmekci, Ayten Kandilci, et al.Clinical Lymphoma, Myeloma & Leukemia|May 16, 2019
The Outcomes of Chronic Myeloid Leukemia Patients With Molecular Warning Responses During Imatinib Treatment According to the European LeukemiaNet 2013 RecommendationsTeoman Soysal, Ahmet Emre Eskazan, Istemi Serin, et al.Genetic Testing and Molecular Biomarkers|October 10, 2009
Comparison of the cytogenetic and molecular analyses in the assessment of imatinib response in chronic myelocytic leukemiaSukru Palanduz, Aysegul Bayrak, Sema Sirma, et al.Pageof 11