Türkyılmaz, A. Et Al. 2023. De novo Pure Partial Trisomy 6p Associated with Facial Dysmorphism, Developmental Delay, Brain Anomalies, and Primary Congenital Hypothyroidism. MOLECULAR SYNDROMOLOGY , vol.14, no.1 , 35-43.

Türkyılmaz, A., Cimbek, E. A., Çebi, A. H., Acar Arslan, E., & Karagüzel, G., (2023). De novo Pure Partial Trisomy 6p Associated with Facial Dysmorphism, Developmental Delay, Brain Anomalies, and Primary Congenital Hypothyroidism. MOLECULAR SYNDROMOLOGY , vol.14, no.1, 35-43.

Türkyılmaz, AYBERK Et Al. "De novo Pure Partial Trisomy 6p Associated with Facial Dysmorphism, Developmental Delay, Brain Anomalies, and Primary Congenital Hypothyroidism," MOLECULAR SYNDROMOLOGY , vol.14, no.1, 35-43, 2023

Türkyılmaz, AYBERK Et Al. "De novo Pure Partial Trisomy 6p Associated with Facial Dysmorphism, Developmental Delay, Brain Anomalies, and Primary Congenital Hypothyroidism." MOLECULAR SYNDROMOLOGY , vol.14, no.1, pp.35-43, 2023

Türkyılmaz, A. Et Al. (2023) . "De novo Pure Partial Trisomy 6p Associated with Facial Dysmorphism, Developmental Delay, Brain Anomalies, and Primary Congenital Hypothyroidism." MOLECULAR SYNDROMOLOGY , vol.14, no.1, pp.35-43.

@article{article, author={AYBERK TÜRKYILMAZ Et Al. }, title={De novo Pure Partial Trisomy 6p Associated with Facial Dysmorphism, Developmental Delay, Brain Anomalies, and Primary Congenital Hypothyroidism}, journal={MOLECULAR SYNDROMOLOGY}, year=2023, pages={35-43} }