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Behavioral and Brain Functions : BBF|May 29, 2010
Two four-marker haplotypes on 7q36.1 region indicate that the potassium channel gene HERG1 (KCNH2, Kv11.1) is related to schizophrenia: a case control studyFatmahan Atalar, Tufan Tevfik Acuner, Naci Cine, et al.
Annals of Human Genetics|December 23, 2011
Estimating the allele frequency of autosomal recessive disorders through mutational records and consanguinity: the Homozygosity Index (HI)Alessandro Gialluisi, Tommaso Pippucci, Yair Anikster, et al.
American Journal of Hematology|February 23, 2007
The SOCS-1 gene methylation in chronic myeloid leukemia patientsOzden Hatirnaz, Umit Ure, Cem Ar, et al.
Digestive Diseases and Sciences|April 6, 2007
HFE gene mutation, chronic liver disease, and iron overload In TurkeyOya Yönal, Ozden Hatirnaz, Filiz Akyüz, et al.
Experimental & Molecular Medicine|July 24, 2004
Real-Time PCR analysis of af4 and dek genes expression in acute promyelocytic leukemia t (15;17) patientsHakan Savli, Sema Sirma, Balint Nagy, et al.
The International Journal of Medical Robotics + Computer Assisted Surgery : MRCAS|May 24, 2007
Robotics in cardiac surgery: the Istanbul experienceErtan Sagbas, Belhhan Akpinar, Ilhan Sanisoglu, et al.
Acta Neurologica Belgica|December 28, 2014
Investigation of the possible association of NEDD4-2 (NEDD4L) gene with idiopathic photosensitive epilepsyEbru Nur Vanli-Yavuz, Ozkan Ozdemir, Ayse Demirkan, et al.
The Heart Surgery Forum|April 12, 2002
The use of stentless valves for root replacement during repair of ascending aortic aneurysms with aortic valve regurgitationBelhhan Akpinar, Mustafa Güden, Saide Aytekin, et al.
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