ÇARMAN, K. B. Et Al. 2022. Wiedemann-Steiner Syndrome: A Rare Differential Diagnosis of Neurodevelopmental Delay and Dysmorphic Features. JOURNAL OF PEDIATRIC GENETICS , vol.11, no.02 , 162-164.

ÇARMAN, K. B., Kaplan, E., Aslan, C. N., Kocagil, S., Cilinigr, O., & YARAR, C., (2022). Wiedemann-Steiner Syndrome: A Rare Differential Diagnosis of Neurodevelopmental Delay and Dysmorphic Features. JOURNAL OF PEDIATRIC GENETICS , vol.11, no.02, 162-164.

ÇARMAN, KÜRŞAT Et Al. "Wiedemann-Steiner Syndrome: A Rare Differential Diagnosis of Neurodevelopmental Delay and Dysmorphic Features," JOURNAL OF PEDIATRIC GENETICS , vol.11, no.02, 162-164, 2022

ÇARMAN, KÜRŞAT B. Et Al. "Wiedemann-Steiner Syndrome: A Rare Differential Diagnosis of Neurodevelopmental Delay and Dysmorphic Features." JOURNAL OF PEDIATRIC GENETICS , vol.11, no.02, pp.162-164, 2022

ÇARMAN, K. B. Et Al. (2022) . "Wiedemann-Steiner Syndrome: A Rare Differential Diagnosis of Neurodevelopmental Delay and Dysmorphic Features." JOURNAL OF PEDIATRIC GENETICS , vol.11, no.02, pp.162-164.

@article{article, author={KÜRŞAT BORA ÇARMAN Et Al. }, title={Wiedemann-Steiner Syndrome: A Rare Differential Diagnosis of Neurodevelopmental Delay and Dysmorphic Features}, journal={JOURNAL OF PEDIATRIC GENETICS}, year=2022, pages={162-164} }