TÜRKYILMAZ, A. Et Al. 2020. FGF3 RELATED PHENOTYPES : A STUDY OF LAMM SYNDROME AND OTODENTAL DYSPLASIA PATIENTS WITH TWO NOVEL MUTATIONS IN FGF3 GENE. International Journal of Human Genetics , vol.20, no.4 , 179-190.

TÜRKYILMAZ, A., GEÇKİNLİ, B. B., ALAVANDA, C., ZENGİN, G., ARSLAN ATEŞ, E., & ARMAN, A., (2020). FGF3 RELATED PHENOTYPES : A STUDY OF LAMM SYNDROME AND OTODENTAL DYSPLASIA PATIENTS WITH TWO NOVEL MUTATIONS IN FGF3 GENE. International Journal of Human Genetics , vol.20, no.4, 179-190.

TÜRKYILMAZ, AYBERK Et Al. "FGF3 RELATED PHENOTYPES : A STUDY OF LAMM SYNDROME AND OTODENTAL DYSPLASIA PATIENTS WITH TWO NOVEL MUTATIONS IN FGF3 GENE," International Journal of Human Genetics , vol.20, no.4, 179-190, 2020

TÜRKYILMAZ, AYBERK Et Al. "FGF3 RELATED PHENOTYPES : A STUDY OF LAMM SYNDROME AND OTODENTAL DYSPLASIA PATIENTS WITH TWO NOVEL MUTATIONS IN FGF3 GENE." International Journal of Human Genetics , vol.20, no.4, pp.179-190, 2020

TÜRKYILMAZ, A. Et Al. (2020) . "FGF3 RELATED PHENOTYPES : A STUDY OF LAMM SYNDROME AND OTODENTAL DYSPLASIA PATIENTS WITH TWO NOVEL MUTATIONS IN FGF3 GENE." International Journal of Human Genetics , vol.20, no.4, pp.179-190.

@article{article, author={AYBERK TÜRKYILMAZ Et Al. }, title={FGF3 RELATED PHENOTYPES : A STUDY OF LAMM SYNDROME AND OTODENTAL DYSPLASIA PATIENTS WITH TWO NOVEL MUTATIONS IN FGF3 GENE}, journal={International Journal of Human Genetics}, year=2020, pages={179-190} }