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Nigerian Journal of Clinical Practice|November 1, 2011
Prevalence of oral mucosal lesions from birth to two yearsA E Yilmaz, C Gorpelioglu, E Sarifakioglu, et al.
Human Heredity|May 1, 1995
Study of 12 mutations in Turkish cystic fibrosis patientsE Yilmaz, H Erdem, M Ozgüç, et al.
The Turkish Journal of Pediatrics|April 1, 1991
Prenatal diagnosis of cystic fibrosis in a Turkish familyE Yilmaz, M Ozgüç, T Coşkun, et al.
Bratislavske Lekarske Listy|April 15, 2015
Serum omentin levels predicts mesenteric ischemiaM Sit, G Aktas, E E Yilmaz, et al.
Genetic Epidemiology|November 17, 2019
Powerful rare variant association testing in a copula-based joint analysis of multiple phenotypesStefan Konigorski, Yildiz E Yilmaz, Jürgen Janke, et al.
Annals of the Rheumatic Diseases|October 2, 2004
E148Q is a disease-causing MEFV mutation: a phenotypic evaluation in patients with familial Mediterranean feverR Topaloglu, F Ozaltin, E Yilmaz, et al.
The Journal of International Medical Research|October 12, 2011
Predictive value of Doppler ultrasound in childhood pneumoniaE Yekeler, A Ucar, R Yilmaz, et al.
The Turkish Journal of Pediatrics|October 1, 1996
Diagnosis of childhood tuberculosis by polymerase chain reactionM Ceyhan, G Kanra, G Seçmeer, et al.
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