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Pediatrics International : Official Journal of the Japan Pediatric Society|August 13, 2003
Celiac disease in children with Down syndrome: importance of follow-up and serologic screeningOzgur Cogulu, Ferda Ozkinay, Cumhur Gunduz, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|December 15, 2010
Mannose-binding lectin codon 54 gene polymorphism in relation to risk of nosocomial invasive fungal infection in preterm neonates in the neonatal intensive care unitCumhur Aydemir, Huseyin Onay, Serife Suna Oguz, et al.
Genetic Testing and Molecular Biomarkers|April 18, 2009
The evaluation of the referral reasons of patients at a tertiary pediatric genetic center in Izmir, TurkeyBurak Durmaz, Asude Alpman, Erhan Pariltay, et al.
European Journal of Medical Genetics|September 13, 2022
LSM1 is the new candidate gene for neurodevelopmental disorderGizem Kok Kilic, Esra Isik, Omer Alpay, et al.
European Journal of Pediatrics|December 25, 2008
Pachyonychia congenita type 2, N92S mutation of keratin 17 gene: clinical features, mutation analysis and pathological viewOzgur Cogulu, Huseyin Onay, Ayca Aykut, et al.
American Journal of Medical Genetics. Part A|April 14, 2017
A further family of Stromme syndrome carrying CENPF mutationFerda Ozkinay, Tahir Atik, Esra Isik, et al.
Clinical Pediatrics|October 4, 2017
Brain Abscess in Children: A Rare but Serious InfectionZumrut Sahbudak Bal, Cenk Eraslan, Elif Bolat, et al.
Neonatology|May 11, 2010
Mannose-binding lectin gene polymorphism and early neonatal outcome in preterm infantsOzge Altun Koroglu, Huseyin Onay, Gulin Erdemir, et al.
Pediatric Research|May 7, 2014
Association of vitamin D receptor gene polymorphisms and bronchopulmonary dysplasiaOzge Altun Koroglu, Huseyin Onay, Bilin Cakmak, et al.
Echocardiography (Mount Kisco, N.Y.)|June 20, 2019
Native valve endocarditis due to Candida albicans in two children: Two new case reportsGizem Guner, Zumrut Sahbudak Bal, Eser Dogan, et al.
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