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Clinical Neurology and Neurosurgery|July 1, 2018
Clinical and genetic features of L1 syndrome patients: Definition of two novel mutationsEsra Isik, Huseyin Onay, Tahir Atik, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|December 8, 2011
A novel homozygous HESX1 mutation causes panhypopituitarism without midline defects and optic nerve anomaliesBurak Durmaz, Ozgur Cogulu, Ceyhun Dizdarer, et al.The Journal of Clinical Pediatric Dentistry|July 30, 2016
The Role of Vitamin D Receptor Polymorphisms on Dental CariesDilsah Cogulu, Huseyin Onay, Yasemin Ozdemir, et al.Archives of Iranian Medicine|June 26, 2012
Mid-trimester hyperechogenic bowel in a fetus of Turkish origin carrying a rarely seen mutation of cystic fibrosisMert Kazandi, Volkan Turan, Gulsah Selvi Demirtas, et al.Pediatric Nephrology (Berlin, Germany)|September 28, 2011
Vitamin D receptor gene polymorphism in children with urinary tract infectionSule Aslan, Ipek Akil, Gulcin Aslan, et al.Molecular Immunology|April 15, 2005
Might there be a link between mannose-binding lectin polymorphism and dental caries?Sacide Pehlivan, Guldane Koturoglu, Ferda Ozkinay, et al.The Turkish Journal of Pediatrics|October 26, 2012
Mannose-binding lectin gene codon 54 polymorphism susceptible to brucellosis in Turkish childrenNuri Bayram, Ferda Ozkinay, Hüseyin Onay, et al.The Turkish Journal of Pediatrics|August 19, 2003
Achondroplasia in Turkey is defined by recurrent G380R mutation of the FGFR3 geneSacide Pehlivan, Ferda Ozkinay, Ozlem Okutman, et al.Pediatric Neurology|January 13, 2009
Febrile seizures: interleukin 1beta and interleukin-1 receptor antagonist polymorphismsGul Serdaroğlu, Asude Alpman, Ayse Tosun, et al.European Journal of Dermatology : EJD|January 9, 2009
Association between IL4 (-590), ACE (I)/(D), CCR5 (Delta32), CTLA4 (+49) and IL1-RN (VNTR in intron 2) gene polymorphisms and vitiligoSacide Pehlivan, Ferda Ozkinay, Sibel Alper, et al.Pageof 15