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Exome sequencing identifies novel NTRK1 mutations in patients with HSAN-IV phenotype.
Altassan R, Saud HA, Masoodi TA, Dosssari HA, Khalifa O, Al-Zaidan H, Sakati N, Rhabeeni Z, Al-Hassnan Z, Binamer Y, Alhashemi N, Wade W, Al-Zayed Z, Al-Sayed M, Al-Muhaizea MA, Meyer B, Al-Owain M, Wakil SM. Altassan R, et al. Am J Med Genet A. 2017 Apr;173(4):1009-1016. doi: 10.1002/ajmg.a.38120. Am J Med Genet A. 2017. PMID: 28328124
Is It Safe for Trainees to Perform Single-Incision Pediatric Endosurgery Splenectomy?
Raboei E, Owiwi Y, Ghallab A, Zeinelabdeen A, Alsaggaf A, Zaidan M, Fayez M, Alawi A, Atta A, Al Fageeh A, Al Fifi K, Al Sayegh M, Banaja A, Haddad A, Al Nefai Z, Aloufi T, Alghamdi S, Abdulrahim I, Al Manea A, Alharbi I, Sait A, Fallatah R. Raboei E, et al. J Laparoendosc Adv Surg Tech A. 2019 Mar;29(3):420-423. doi: 10.1089/lap.2018.0530. Epub 2018 Dec 5. J Laparoendosc Adv Surg Tech A. 2019. PMID: 30517054
Further delineation of van den Ende-Gupta syndrome: Genetic heterogeneity and overlap with congenital heart defects and skeletal malformations syndrome.
Hildebrandt CC, Patel N, Graham JM Jr, Bamshad M, Nickerson DA, White JJ, Marvin CT, Miller DE; University of Washington Center for Mendelian Genomics; Grand KL, Sanchez-Lara PA, Schweitzer D, Al-Zaidan HI, Al Masseri Z, Alkuraya FS, Lin AE. Hildebrandt CC, et al. Am J Med Genet A. 2021 Jul;185(7):2136-2149. doi: 10.1002/ajmg.a.62194. Epub 2021 Mar 30. Am J Med Genet A. 2021. PMID: 33783941