AKALIN, A. Et Al. 2023. Typical Face, Developmental Delay, and Hearing Loss in a Patient with 3M Syndrome: The Co-Occurrence of Two Rare Conditions. MOLECULAR SYNDROMOLOGY , vol.13, no.6 , 537-542.

AKALIN, A., Simsek-Kiper, P. O., Taskiran, E., ÜTİNE, G. E., & BODUROĞLU, O. K., (2023). Typical Face, Developmental Delay, and Hearing Loss in a Patient with 3M Syndrome: The Co-Occurrence of Two Rare Conditions. MOLECULAR SYNDROMOLOGY , vol.13, no.6, 537-542.

AKALIN, AKÇAHAN Et Al. "Typical Face, Developmental Delay, and Hearing Loss in a Patient with 3M Syndrome: The Co-Occurrence of Two Rare Conditions," MOLECULAR SYNDROMOLOGY , vol.13, no.6, 537-542, 2023

AKALIN, AKÇAHAN Et Al. "Typical Face, Developmental Delay, and Hearing Loss in a Patient with 3M Syndrome: The Co-Occurrence of Two Rare Conditions." MOLECULAR SYNDROMOLOGY , vol.13, no.6, pp.537-542, 2023

AKALIN, A. Et Al. (2023) . "Typical Face, Developmental Delay, and Hearing Loss in a Patient with 3M Syndrome: The Co-Occurrence of Two Rare Conditions." MOLECULAR SYNDROMOLOGY , vol.13, no.6, pp.537-542.

@article{article, author={AKÇAHAN AKALIN Et Al. }, title={Typical Face, Developmental Delay, and Hearing Loss in a Patient with 3M Syndrome: The Co-Occurrence of Two Rare Conditions}, journal={MOLECULAR SYNDROMOLOGY}, year=2023, pages={537-542} }