APA (7th ed.) Citation

Singin, B., Donbaloğlu, Z., Çetiner, E. B., Bedel, A., Çetin, K., Paksoy, B. A., . . . Parlak, M. (2026). 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, 18, 83. https://doi.org/10.4274/jcrpe.galenos.2025.2024-12-4

Chicago Style (17th ed.) Citation

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 18 (2026): 83. https://doi.org/10.4274/jcrpe.galenos.2025.2024-12-4.

MLA (9th ed.) Citation

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, vol. 18, 2026, p. 83, https://doi.org/10.4274/jcrpe.galenos.2025.2024-12-4.