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Page 1
Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8.
Boycott KM, Beaulieu CL, Kernohan KD, Gebril OH, Mhanni A, Chudley AE, Redl D, Qin W, Hampson S, Küry S, Tetreault M, Puffenberger EG, Scott JN, Bezieau S, Reis A, Uebe S, Schumacher J, Hegele RA, McLeod DR, Gálvez-Peralta M, Majewski J, Ramaekers VT; Care4Rare Canada Consortium; Nebert DW, Innes AM, Parboosingh JS, Abou Jamra R. Boycott KM, et al. Among authors: gebril oh. Am J Hum Genet. 2015 Dec 3;97(6):886-93. doi: 10.1016/j.ajhg.2015.11.002. Am J Hum Genet. 2015. PMID: 26637978 Free PMC article.
Johnson-McMillin Microtia Syndrome: New Additional Family.
Abdel-Meguid N, Gebril OH, Abdelraouf ER, Shafie MA, Bahgat M. Abdel-Meguid N, et al. Among authors: gebril oh. J Family Med Prim Care. 2014 Jul;3(3):275-8. doi: 10.4103/2249-4863.141639. J Family Med Prim Care. 2014. PMID: 25374870 Free PMC article.
Brain haemosiderin in older people: pathological evidence for an ischaemic origin of magnetic resonance imaging (MRI) microbleeds.
Janaway BM, Simpson JE, Hoggard N, Highley JR, Forster G, Drew D, Gebril OH, Matthews FE, Brayne C, Wharton SB, Ince PG; MRC Cognitive Function and Ageing Neuropathology Study. Janaway BM, et al. Among authors: gebril oh. Neuropathol Appl Neurobiol. 2014 Apr;40(3):258-69. doi: 10.1111/nan.12062. Neuropathol Appl Neurobiol. 2014. PMID: 23678850 Free PMC article.