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Year | Number of Results |
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Page 1
Congenital disorders of glycosylation: The Saudi experience.
Am J Med Genet A. 2017 Oct;173(10):2614-2621. doi: 10.1002/ajmg.a.38358. Epub 2017 Jul 25.
Am J Med Genet A. 2017.
PMID: 28742265
Common disease-associated gene variants in a Saudi Arabian population.
Aleissa M, Aloraini T, Alsubaie LF, Hassoun M, Abdulrahman G, Swaid A, Eyaid WA, Mutairi FA, Ababneh F, Alfadhel M, Alfares A.
Aleissa M, et al. Among authors: mutairi fa.
Ann Saudi Med. 2022 Jan-Feb;42(1):29-35. doi: 10.5144/0256-4947.2022.29. Epub 2022 Feb 3.
Ann Saudi Med. 2022.
PMID: 35112591
Free PMC article.
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Whole-genome sequencing offers additional but limited clinical utility compared with reanalysis of whole-exome sequencing.
Alfares A, Aloraini T, Subaie LA, Alissa A, Qudsi AA, Alahmad A, Mutairi FA, Alswaid A, Alothaim A, Eyaid W, Albalwi M, Alturki S, Alfadhel M.
Alfares A, et al. Among authors: mutairi fa.
Genet Med. 2018 Nov;20(11):1328-1333. doi: 10.1038/gim.2018.41. Epub 2018 Mar 22.
Genet Med. 2018.
PMID: 29565419
Free article.
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Guidelines for acute management of hyperammonemia in the Middle East region.
Alfadhel M, Mutairi FA, Makhseed N, Jasmi FA, Al-Thihli K, Al-Jishi E, AlSayed M, Al-Hassnan ZN, Al-Murshedi F, Häberle J, Ben-Omran T.
Alfadhel M, et al. Among authors: mutairi fa.
Ther Clin Risk Manag. 2016 Mar 31;12:479-87. doi: 10.2147/TCRM.S93144. eCollection 2016.
Ther Clin Risk Manag. 2016.
PMID: 27099506
Free PMC article.
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Further Delineation of the Clinical Phenotype of Cerebellar Ataxia, Mental Retardation, and Disequilibrium Syndrome Type 4.
Alsahli S, Alrifai MT, Al Tala S, Mutairi FA, Alfadhel M.
Alsahli S, et al. Among authors: mutairi fa.
J Cent Nerv Syst Dis. 2018 Feb 28;10:1179573518759682. doi: 10.1177/1179573518759682. eCollection 2018.
J Cent Nerv Syst Dis. 2018.
PMID: 29531481
Free PMC article.
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Mutation in SLC6A9 encoding a glycine transporter causes a novel form of non-ketotic hyperglycinemia in humans.
Alfadhel M, Nashabat M, Qahtani HA, Alfares A, Mutairi FA, Shaalan HA, Douglas GV, Wierenga K, Juusola J, Alrifai MT, Arold ST, Alkuraya F, Ali QA.
Alfadhel M, et al. Among authors: mutairi fa.
Hum Genet. 2016 Nov;135(11):1263-1268. doi: 10.1007/s00439-016-1719-x. Epub 2016 Aug 1.
Hum Genet. 2016.
PMID: 27481395
Free PMC article.
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