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Genetic Counseling (Geneva, Switzerland)|March 26, 2015
A twin sibling with Prader-Willi syndrome caused by uniparental disomy conceived after in vitro fertilizationT Atik, A Aykut, E Karaca, et al.Andrologia|May 3, 2016
A novel mutation in steroidogenic factor (SF1/NR5A1) gene in a patient with 46 XY DSD without adrenal insufficiencyH Tuhan, A Anik, G Catli, et al.Journal Francais D'Ophtalmologie|November 2, 2023
Dysfunctional personality beliefs and psychopathology in patients with central serous chorioretinopathyF Çam, M O Sevik, A Aykut, et al.Gene|April 27, 2013
Analysis of the sphingomyelin phosphodiesterase 1 gene (SMPD1) in Turkish Niemann-Pick disease patients: mutation profile and description of a novel mutationA Aykut, E Karaca, H Onay, et al.American Journal of Respiratory and Critical Care Medicine|July 21, 2001
"Natural history" of pulmonary hypertension in a series of 131 patients with chronic obstructive lung diseaseR Kessler, M Faller, E Weitzenblum, et al.Genetic Counseling (Geneva, Switzerland)|April 25, 2013
Genome wide analysis in a discordant monozygotic twin with caudal appendage and multiple congenital anomaliesO Cogulu, E Pariltay, O A Koroglu, et al.Respiratory Medicine|July 1, 1997
Post-traumatic pleural effusion: demonstration of local complement consumptionF de Blay, A Aykut-Baturalp, J Goetz, et al.Annales De Cardiologie Et D'Angeiologie|June 15, 2007
[Surgery of cardiac hydatid cysts. Experience of 39 years]G Orhan, B Ozay, Z Tartan, et al.Genetic Counseling (Geneva, Switzerland)|July 26, 2014
Genome-wide copy number variation analysis in idiopathic intellectual disability/multiple congenital anomaliesE Pariltay, A Durmaz, B Durmaz, et al.Pageof 2