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Prenatal Diagnosis|April 4, 2003
A familial Xp+ chromosome detected during fetal karyotyping, which is associated with short stature in four generations of a Turkish familyB Karaman, B Wollnik, H Ermiş, et al.European Review for Medical and Pharmacological Sciences|September 5, 2023
Are orthopedic surgeons able to detect 3 mm and 5 mm joint step off on fluoroscopy?A Oztermeli, O Karakus, A S SariEuropean Journal of Paediatric Dentistry|August 8, 2014
Treatment of horizontal root fractured central incisors and 30 months follow up: 2 case reportsV Arikan, Z K Celikten, S SariHereditas|October 7, 1998
An unusual translocation between 12tel and 14q11 in a large kindredS Palanduz, D Ustek, B Karaman, et al.The British Journal of Radiology|June 17, 2010
Anatomical variations of hepatic arterial system, coeliac trunk and renal arteries: an analysis with multidetector CT angiographyM S Ugurel, B Battal, U Bozlar, et al.Genetic Counseling (Geneva, Switzerland)|September 10, 2015
PRENATAL DIAGNOSIS OF DE NOVO PERICENTRIC INVERSION INV(2)(p11.2z13)S Yakut, Z Cetin, C Sanhal, et al.Genetic Counseling (Geneva, Switzerland)|December 3, 2015
PRENATAL DIAGNOSIS OF DE NOVO SUPERNUMERARY MARKER CHROMOSOME ORIGINATED FROM CHROMOSOME 16 BY ARRAY-CGHS Yakut, Z Cetin, C Sanhal, et al.Balkan Journal of Medical Genetics : BJMG|September 21, 2013
Turner Syndrome with Isochromosome Xq and Familial Reciprocal Translocation t(4;16)(p15.2;p13.1)Z Cetin, I Mendilcioglu, S Yakut, et al.Journal of Oral Rehabilitation|June 8, 2001
Prevalence of temporomandibular dysfunction in Turkish children with mixed and permanent dentitionH Sönmez, S Sari, G Oksak Oray, et al.The Journal of Clinical Pediatric Dentistry|March 10, 2000
Temporomandibular joint dysfunction and occlusion in the mixed and permanent dentitionS Sari, H Sonmez, G O Oray, et al.Pageof 7