Singin, B. Et Al. 2025. Xp21 Contiguous Gene Deletion Syndrome: Diagnosis, Treatment, and a Review of the Literature on a Rare Genetic Disorder.. Journal of clinical research in pediatric endocrinology .

Singin, B., Donbaloğlu, Z., Barsal Çetiner, E., Bedel, A., Çetin, K., Akcan Paksoy, B., ... Kalkan, T.(2025). Xp21 Contiguous Gene Deletion Syndrome: Diagnosis, Treatment, and a Review of the Literature on a Rare Genetic Disorder.. Journal of clinical research in pediatric endocrinology .

Singin, Berna Et Al. "Xp21 Contiguous Gene Deletion Syndrome: Diagnosis, Treatment, and a Review of the Literature on a Rare Genetic Disorder.," Journal of clinical research in pediatric endocrinology , 2025

Singin, Berna Et Al. "Xp21 Contiguous Gene Deletion Syndrome: Diagnosis, Treatment, and a Review of the Literature on a Rare Genetic Disorder.." Journal of clinical research in pediatric endocrinology , 2025

Singin, B. Et Al. (2025) . "Xp21 Contiguous Gene Deletion Syndrome: Diagnosis, Treatment, and a Review of the Literature on a Rare Genetic Disorder.." Journal of clinical research in pediatric endocrinology .

@article{article, author={Berna Singin Et Al. }, title={Xp21 Contiguous Gene Deletion Syndrome: Diagnosis, Treatment, and a Review of the Literature on a Rare Genetic Disorder.}, journal={Journal of clinical research in pediatric endocrinology}, year=2025}