Kamal, N. M., Sahly, A. N., Banaganapalli, B., Rashidi, O. M., Shetty, P. J., Al-Aama, J. Y., . . . Saadah, O. I. (2020). Whole exome sequencing identifies rare biallelic ALMS1 missense and stop gain mutations in familial Alström syndrome patients. Saudi J Biol Sci.

Kamal, Naglaa M., Ahmed N. Sahly, Babajan Banaganapalli, Omran M. Rashidi, Preetha J. Shetty, Jumana Y. Al-Aama, Noor A. Shaik, Ramu Elango, and Omar I. Saadah. "Whole Exome Sequencing Identifies Rare Biallelic ALMS1 Missense and Stop Gain Mutations in Familial Alström Syndrome Patients." Saudi J Biol Sci 2020.

Kamal, Naglaa M., et al. "Whole Exome Sequencing Identifies Rare Biallelic ALMS1 Missense and Stop Gain Mutations in Familial Alström Syndrome Patients." Saudi J Biol Sci 2020.