H. MUTLU ALBAYRAK Et Al. , "A case of Crouzon syndrome with mild phenotypic features and FGFR2 Y328C mutation," Medical Genetics and Clinical Applications (with International Participation) , vol.1, 2016
MUTLU ALBAYRAK, H. Et Al. 2016. A case of Crouzon syndrome with mild phenotypic features and FGFR2 Y328C mutation. Medical Genetics and Clinical Applications (with International Participation) .
MUTLU ALBAYRAK, H., SANRI, A., Durmaz, A., AYKUT, A., YALÇIN, H. Y., & OĞUR, M. G., (2016). A case of Crouzon syndrome with mild phenotypic features and FGFR2 Y328C mutation . Medical Genetics and Clinical Applications (with International Participation)
MUTLU ALBAYRAK, HATİCE Et Al. "A case of Crouzon syndrome with mild phenotypic features and FGFR2 Y328C mutation," Medical Genetics and Clinical Applications (with International Participation), 2016
MUTLU ALBAYRAK, HATİCE Et Al. "A case of Crouzon syndrome with mild phenotypic features and FGFR2 Y328C mutation." Medical Genetics and Clinical Applications (with International Participation) , 2016
MUTLU ALBAYRAK, H. Et Al. (2016) . "A case of Crouzon syndrome with mild phenotypic features and FGFR2 Y328C mutation." Medical Genetics and Clinical Applications (with International Participation) .
@conferencepaper{conferencepaper, author={HATİCE MUTLU Et Al. }, title={A case of Crouzon syndrome with mild phenotypic features and FGFR2 Y328C mutation}, congress name={Medical Genetics and Clinical Applications (with International Participation)}, city={}, country={}, year={2016}}