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Methods in Molecular Biology (Clifton, N.J.)|January 5, 2011
Genetic predisposition to β-thalassemia and sickle cell anemia in Turkey: a molecular diagnostic approachA Nazli Basak, Sukru Tuzmen
British Journal of Haematology|December 11, 2002
A 3'UTR mutation affects beta-globin expression without altering the stability of its fully processed mRNAOnur Bilenoglu, A Nazli Basak, J Eric Russell
Hemoglobin|August 7, 2009
Is the frameshift codons 8/9 (+G) [FSC 8/9 (+G)] beta-thalassemia mutation, detected by the polymerase chain reaction-amplification refractory mutation system, really FSC 8/9 (+G)?Mehdi Haghi, Abbas Ali Hosseinpour Feizi, Mohammad Ali Hosseinpour Feizi, et al.
Journal of the Neurological Sciences|October 23, 2009
Combination of myotonic dystrophy and hereditary motor and sensory neuropathySemiha Kurt, Hatice Karaer, Yuksel Kaplan, et al.
Pediatric Blood & Cancer|June 19, 2008
Coinheritance of sickle cell anemia and hereditary spherocytosisNilgun Selcuk Duru, Tiraje Celkan, Mahmut Civilibal, et al.
Case Reports in Neurological Medicine|September 27, 2016
Atypical Features in a Large Turkish Family Affected with Friedreich AtaxiaSemiha Kurt, Betul Cevik, Durdane Aksoy, et al.
Journal of the Neurological Sciences|November 13, 2008
Delayed diagnosis of a neuroBehçet patient with only brainstem and cerebellar atrophy: literature reviewOzlem Taskapilioglu, Meral Seferoglu, Cengiz Akkaya, et al.
The Heart Surgery Forum|November 1, 2017
Impact of Genetic Defects on Coronary Atherosclerosis among Turkish CypriotsCenk Conkbayir, Rezan Fahrioglu Yamaci, Pinar Gencer, et al.
Elife|January 27, 2026
Directed differentiation of functional corticospinal-like neurons from endogenous SOX6+/NG2+ cortical progenitorsAbdulkadir Ozkan, Hari K Padmanabhan, Seth L Shipman, et al.
Biorxiv : the Preprint Server for Biology|May 7, 2024
Directed differentiation of functional corticospinal-like neurons from endogenous SOX6+/NG2+ cortical progenitorsAbdulkadir Ozkan, Hari K Padmanabhan, Seth L Shipman, et al.
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