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Epilepsy Research|May 20, 2015
A clinical variant in SCN1A inherited from a mosaic father cosegregates with a novel variant to cause Dravet syndrome in a consanguineous familyFeyza N Tuncer, Zeliha Gormez, Mustafa Calik, et al.
Scientific Reports|July 7, 2025
Aryl hydrocarbon receptor interacting protein and syndromic gene variants detected in Turkish isolated pituitary adenoma families by whole exome sequencingM Eda Ertorer, Feyza N Tuncer, Sema Ciftci, et al.
Turk Gogus Kalp Damar Cerrahisi Dergisi|June 27, 2024
Second harvest of Congenital Heart Surgery Database in Türkiye: Current outcomesErsin Erek, Serdar Başgöze, Okan Yıldız, et al.
Molecular Genetics and Metabolism|April 12, 2015
Practices in prescribing protein substitutes for PKU in Europe: No uniformity of approachA Aguiar, K Ahring, M F Almeida, et al.
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