APA (7th ed.) Citation

Al‐Azri, F., Al‐Rashdi, M., Al‐Murshedi, F., Otaify, G. A., Al‐Jabry, T., Al‐Kindi, A., . . . Al‐Maawali, A. (2026). Biallelic XPR1 Variants Are Linked to Brain Calcifications, Developmental Delay, Hypophosphatemia, and Cardiopulmonary Phenotype. Clinical Genetics, 110(1), 102. https://doi.org/10.1111/cge.70161

Chicago Style (17th ed.) Citation

Al‐Azri, Fakhriya, Maryam Al‐Rashdi, Fathiya Al‐Murshedi, Ghada A. Otaify, Tariq Al‐Jabry, Adila Al‐Kindi, Sobia Ahsan Halim, Ahmed Al‐Harrasi, and Almundher Al‐Maawali. "Biallelic XPR1 Variants Are Linked to Brain Calcifications, Developmental Delay, Hypophosphatemia, and Cardiopulmonary Phenotype." Clinical Genetics 110, no. 1 (2026): 102. https://doi.org/10.1111/cge.70161.

MLA (9th ed.) Citation

Al‐Azri, Fakhriya, et al. "Biallelic XPR1 Variants Are Linked to Brain Calcifications, Developmental Delay, Hypophosphatemia, and Cardiopulmonary Phenotype." Clinical Genetics, vol. 110, no. 1, 2026, p. 102, https://doi.org/10.1111/cge.70161.