E. ALTUNDAĞ Et Al. , "Association of developmental delay, congenital adrenal hypoplasia, duchenne muscular dystrophy and glycerol kinase deficiency: a rare Xp21 contiguous gene deletion syndrome," Erciyes Medical Genetics Days 2017 , vol.39, pp.5000, 2017
ALTUNDAĞ, E. Et Al. 2017. Association of developmental delay, congenital adrenal hypoplasia, duchenne muscular dystrophy and glycerol kinase deficiency: a rare Xp21 contiguous gene deletion syndrome. Erciyes Medical Genetics Days 2017 , 5000.
ALTUNDAĞ, E., KARA, C., SANRI, A., MUTLU ALBAYRAK, H., YALÇIN, H. Y., & OĞUR, M. G., (2017). Association of developmental delay, congenital adrenal hypoplasia, duchenne muscular dystrophy and glycerol kinase deficiency: a rare Xp21 contiguous gene deletion syndrome . Erciyes Medical Genetics Days 2017 (pp.5000).
ALTUNDAĞ, ENGİN Et Al. "Association of developmental delay, congenital adrenal hypoplasia, duchenne muscular dystrophy and glycerol kinase deficiency: a rare Xp21 contiguous gene deletion syndrome," Erciyes Medical Genetics Days 2017, 2017
ALTUNDAĞ, ENGİN Et Al. "Association of developmental delay, congenital adrenal hypoplasia, duchenne muscular dystrophy and glycerol kinase deficiency: a rare Xp21 contiguous gene deletion syndrome." Erciyes Medical Genetics Days 2017 , pp.5000, 2017
ALTUNDAĞ, E. Et Al. (2017) . "Association of developmental delay, congenital adrenal hypoplasia, duchenne muscular dystrophy and glycerol kinase deficiency: a rare Xp21 contiguous gene deletion syndrome." Erciyes Medical Genetics Days 2017 , p.5000.
@conferencepaper{conferencepaper, author={ENGİN ALTUNDAĞ Et Al. }, title={Association of developmental delay, congenital adrenal hypoplasia, duchenne muscular dystrophy and glycerol kinase deficiency: a rare Xp21 contiguous gene deletion syndrome}, congress name={Erciyes Medical Genetics Days 2017}, city={}, country={}, year={2017}, pages={5000} }