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Molecular diagnosis of fragile X syndrome using methylation sensitive techniques in a cohort of patients with intellectual disability.
Chaudhary AG, Hussein IR, Abuzenadah A, Gari M, Bassiouni R, Sogaty S, Lary S, Al-Quaiti M, Al Balwi M, Al Qahtani M. Chaudhary AG, et al. Among authors: al quaiti m, al qahtani m, al balwi m. Pediatr Neurol. 2014 Apr;50(4):368-76. doi: 10.1016/j.pediatrneurol.2013.11.020. Epub 2013 Dec 4. Pediatr Neurol. 2014. PMID: 24630283
Prognostic value of mitotic counts in breast cancer of Saudi Arabian patients.
Buhmeida A, Al-Maghrabi J, Merdad A, Al-Thubaity F, Chaudhary A, Gari M, Abuzenadah A, Collan Y, Syrjänen K, Al-Qahtani M. Buhmeida A, et al. Among authors: al maghrabi j, al thubaity f, al qahtani m. Anticancer Res. 2011 Jan;31(1):97-103. Anticancer Res. 2011. PMID: 21273586
Incidence and potential causative factors associated with chronic benign neutropenia in the Kingdom of Saudi Arabia.
Gari M, Dakhakhni M, Gari A, Alshihri E, Al-Jahdali R, Narasimhan K, Liang S, Al-Sayes F, Kalamegam G, Chaudhary A, Abuzenadah A, Al-Qahtani M. Gari M, et al. Among authors: al sayes f, al qahtani m, al jahdali r. BMC Proc. 2015 Jan 15;9(Suppl 2 Selected article from the 2nd International Genomic):S1. doi: 10.1186/1753-6561-9-S2-S1. eCollection 2015. BMC Proc. 2015. PMID: 25810761 Free PMC article.
422 results