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Further delineation of MYO18B-related autosomal recessive Klippel-Feil syndrome with myopathy and facial dysmorphism.
Am J Med Genet A. 2021 Feb;185(2):370-376. doi: 10.1002/ajmg.a.61957. Epub 2020 Nov 11.
Am J Med Genet A. 2021.
PMID: 33179433
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
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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
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Map of autosomal recessive genetic disorders in Saudi Arabia: concepts and future directions.
Al-Owain M, Al-Zaidan H, Al-Hassnan Z.
Al-Owain M, et al.
Am J Med Genet A. 2012 Oct;158A(10):2629-40. doi: 10.1002/ajmg.a.35551. Epub 2012 Aug 17.
Am J Med Genet A. 2012.
PMID: 22903695
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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
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Delineating the phenotypic spectrum of hyperphosphatasia with mental retardation syndrome 4 in 14 patients of Middle-Eastern origin.
Balobaid A, Ben-Omran T, Ramzan K, Altassan R, Almureikhi M, Musa S, Al-Hashmi N, Al-Owain M, Al-Zaidan H, Al-Hassnan Z, Imtiaz F, Al-Sayed M.
Balobaid A, et al.
Am J Med Genet A. 2018 Dec;176(12):2850-2857. doi: 10.1002/ajmg.a.40627. Epub 2018 Oct 22.
Am J Med Genet A. 2018.
PMID: 30345601
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Variation in cottonmouth (Agkistrodon piscivorus leucostoma) resting metabolic rates.
Zaidan F 3rd.
Zaidan F 3rd.
Comp Biochem Physiol A Mol Integr Physiol. 2003 Mar;134(3):511-23. doi: 10.1016/s1095-6433(02)00344-6.
Comp Biochem Physiol A Mol Integr Physiol. 2003.
PMID: 12600660
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