Umm Al-Qura University
Abduljaleel, Z., Al-Allaf, F.A., Khan, W., Athar, M., Shahzad, N., Taher, M.M., Alanazi, M., Elrobh, M. and Reddy, N.P., 2014. DNA mismatch repair MSH2 gene-based SNP associated with different populations. Molecular genetics and genomics, 289(3), pp.469-487.
Abduljaleel, Z., Al-Allaf, F.A., Khan, W., Athar, M., Shahzad, N., Taher, M.M., Elrobh, M., Alanazi, M.S. and El-Huneidi, W., 2014. Evidence of trem2 variant associated with triple risk of Alzheimer’s disease. PLoS One, 9(3).
Abumansour, I.S., Wrogemann, J., Chudley, A.E., Chodirker, B.N. and Salman, M.S., 2014. Lissencephaly with brainstem and cerebellar hypoplasia and congenital cataracts. Journal of child neurology, 29(6), pp.860-864.
