APA

Hashmi J. A., Albarry M. A., Almatrafi A. M., Albalawi A. M., Mahmood A. & Basit S. (20180830). Whole exome sequencing identified a novel single base pair insertion mutation in the EYS gene in a six generation family with retinitis pigmentosa. : Congenital anomalies.

Chicago

Hashmi Jamil Amjad, Albarry Maan Abdullah, Almatrafi Ahmed M, Albalawi Alia M, Mahmood Amer and Basit Sulman. 20180830. Whole exome sequencing identified a novel single base pair insertion mutation in the EYS gene in a six generation family with retinitis pigmentosa. : Congenital anomalies.

Harvard

Hashmi J. A., Albarry M. A., Almatrafi A. M., Albalawi A. M., Mahmood A. and Basit S. (20180830). Whole exome sequencing identified a novel single base pair insertion mutation in the EYS gene in a six generation family with retinitis pigmentosa. : Congenital anomalies.

MLA

Hashmi Jamil Amjad, Albarry Maan Abdullah, Almatrafi Ahmed M, Albalawi Alia M, Mahmood Amer and Basit Sulman. Whole exome sequencing identified a novel single base pair insertion mutation in the EYS gene in a six generation family with retinitis pigmentosa. : Congenital anomalies. 20180830.