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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 RussellMethods 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 TuzmenJapanese Journal of Infectious Diseases|March 24, 2009
Genotyping of Brucella melitensis by rpoB gene analysis and re-evaluation of conventional serotyping methodMurat Sayan, Zeki Yumuk, Onur Bilenoglu, et al.Clinical Laboratory|October 17, 2022
The Prevalence of Protein S Variant in Patients Diagnosed with COVID-19Derya Bayirli-Turan, Mustafa Usanmaz, Selim Gorgun, et al.European Journal of Haematology|November 3, 2007
A post-transcriptional process contributes to efficient gamma-globin gene silencing in definitive erythroid cellsJ Eric RussellHemoglobin|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.Pageof 6