Showing results (21-30 of 50) with videos related to
Sort By:
Pageof 5
Acta Endocrinologica (Bucharest, Romania : 2005)|June 1, 2019
GENETIC DISORDERS OF PITUITARY DEVELOPMENT IN PATIENTS WITH SHEEHAN'S SYNDROMEH Diri, E F Sener, F Bayram, et al.Genetic Counseling (Geneva, Switzerland)|August 19, 2011
Partial trisomy 3q in a child with sacrococcygeal teratoma and Cornelia de Lange syndrome phenotypeM Dundar, A Uzak, M Erdogan, et al.Journal of Endocrinological Investigation|April 13, 2023
Unexpectedly high mutation rate of cyp11b1 compared to cyp21a2 in randomly-selected turkish women: a large screening studyS Polat, S Karaburgu, K Unluhizarci, et al.Balkan Journal of Medical Genetics : BJMG|September 21, 2020
The Effects of O<sup>6</sup>-methyl Guanine DNA-methyl Transferase Promotor Methylation and CpG1, CpG2, CpG3 and CpG4 Methylation on Treatment Response and their Prognostic Significance in Patients with GlioblastomaO G Yildiz, D Aslan, H Akalin, et al.Current Opinion in Biotechnology|June 18, 2011
Biotechnology worldwide and the 'European Biotechnology Thematic Network' Association (EBTNA)F Bruschi, M Dundar, P B Gahan, et al.Genetic Counseling (Geneva, Switzerland)|August 5, 2010
A unique case of a patient with partial trisomy 22 and lipodystrophy: is it a new syndrome due to an IGF-IR mutation?A O Caglayan, J Klammt, W Kiess, et al.Current Opinion in Biotechnology|June 26, 2013
Progress towards the 'Golden Age' of biotechnologyK M A Gartland, F Bruschi, M Dundar, et al.Clinical Dysmorphology|January 11, 2001
A case with Waardenburg syndrome presenting with two separate translocations--one reciprocal and one complexM Dundar, G Lowther, J Colgan, et al.Genetic Counseling (Geneva, Switzerland)|November 11, 2008
Scoliosis, blindness and arachnodactyly in a large Turkish family: is it a new syndrome?M Dundar, K Erkilic, M Argun, et al.The British Journal of Radiology|May 27, 2005
Computer-aided detection (CAD) for CT colonography: a tool to address a growing needL Bogoni, P Cathier, M Dundar, et al.Pageof 5