H. Aylanc Et Al. , "Familial intragenic X-linked OPHN1 gene deletion in a newborn male infant with low birth weight and distinctive facial appearance that diagnosed by advanced microarray-CGH method," Cumhuriyet Tıp Dergisi (ELEKTRONİK) , vol.44, no.1, pp.125-130, 2022
Aylanc, H. Et Al. 2022. Familial intragenic X-linked OPHN1 gene deletion in a newborn male infant with low birth weight and distinctive facial appearance that diagnosed by advanced microarray-CGH method. Cumhuriyet Tıp Dergisi (ELEKTRONİK) , vol.44, no.1 , 125-130.
Aylanc, H., Sılan, F., Çokyaman, T., Akcan, M. B., & Özdemir, Ö., (2022). Familial intragenic X-linked OPHN1 gene deletion in a newborn male infant with low birth weight and distinctive facial appearance that diagnosed by advanced microarray-CGH method. Cumhuriyet Tıp Dergisi (ELEKTRONİK) , vol.44, no.1, 125-130.
Aylanc, HAKAN Et Al. "Familial intragenic X-linked OPHN1 gene deletion in a newborn male infant with low birth weight and distinctive facial appearance that diagnosed by advanced microarray-CGH method," Cumhuriyet Tıp Dergisi (ELEKTRONİK) , vol.44, no.1, 125-130, 2022
Aylanc, HAKAN Et Al. "Familial intragenic X-linked OPHN1 gene deletion in a newborn male infant with low birth weight and distinctive facial appearance that diagnosed by advanced microarray-CGH method." Cumhuriyet Tıp Dergisi (ELEKTRONİK) , vol.44, no.1, pp.125-130, 2022
Aylanc, H. Et Al. (2022) . "Familial intragenic X-linked OPHN1 gene deletion in a newborn male infant with low birth weight and distinctive facial appearance that diagnosed by advanced microarray-CGH method." Cumhuriyet Tıp Dergisi (ELEKTRONİK) , vol.44, no.1, pp.125-130.
@article{article, author={HAKAN AYLANÇ Et Al. }, title={Familial intragenic X-linked OPHN1 gene deletion in a newborn male infant with low birth weight and distinctive facial appearance that diagnosed by advanced microarray-CGH method}, journal={Cumhuriyet Tıp Dergisi (ELEKTRONİK)}, year=2022, pages={125-130} }