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nabil mohammed
(10 results)?
Apolipoprotein E Epsilon 4 Genotype, Mild Traumatic Brain Injury, and the Development of Chronic Traumatic Encephalopathy.
Med Sci (Basel). 2018 Sep 14;6(3):78. doi: 10.3390/medsci6030078.
Med Sci (Basel). 2018.
PMID: 30223506
Free PMC article.
Review.
Nonampullary Duodenal Adenomas in Familial Adenomatous Polyposis and Sporadic Patients Lack the DNA Content Abnormality That Is Characteristic of the Adenoma-Carcinoma Sequence Involved in the Development of Other Gastrointestinal Malignancies.
Mohammed N, Rabinovitch PS, Wang D, Kővári BP, Mattis AN, Lauwers GY, Choi WT.
Mohammed N, et al.
Am J Surg Pathol. 2021 Dec 1;45(12):1694-1702. doi: 10.1097/PAS.0000000000001754.
Am J Surg Pathol. 2021.
PMID: 34138799
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Genetic variation of FOXE1 and risk for orofacial clefts in a California population.
Lammer EJ, Mohammed N, Iovannisci DM, Ma C, Lidral AC, Shaw GM.
Lammer EJ, et al. Among authors: mohammed n.
Am J Med Genet A. 2016 Nov;170(11):2770-2776. doi: 10.1002/ajmg.a.37871. Epub 2016 Sep 8.
Am J Med Genet A. 2016.
PMID: 27604706
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Diacylglycerol kinase K variants impact hypospadias in a California study population.
Carmichael SL, Mohammed N, Ma C, Iovannisci D, Choudhry S, Baskin LS, Witte JS, Shaw GM, Lammer EJ.
Carmichael SL, et al. Among authors: mohammed n.
J Urol. 2013 Jan;189(1):305-11. doi: 10.1016/j.juro.2012.09.002. Epub 2012 Nov 21.
J Urol. 2013.
PMID: 23177175
Free PMC article.
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De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects.
Priest JR, Osoegawa K, Mohammed N, Nanda V, Kundu R, Schultz K, Lammer EJ, Girirajan S, Scheetz T, Waggott D, Haddad F, Reddy S, Bernstein D, Burns T, Steimle JD, Yang XH, Moskowitz IP, Hurles M, Lifton RP, Nickerson D, Bamshad M, Eichler EE, Mital S, Sheffield V, Quertermous T, Gelb BD, Portman M, Ashley EA.
Priest JR, et al. Among authors: mohammed n.
PLoS Genet. 2016 Apr 8;12(4):e1005963. doi: 10.1371/journal.pgen.1005963. eCollection 2016 Apr.
PLoS Genet. 2016.
PMID: 27058611
Free PMC article.
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Haploinsufficiency of insulin gene enhancer protein 1 (ISL1) is associated with d-transposition of the great arteries.
Osoegawa K, Schultz K, Yun K, Mohammed N, Shaw GM, Lammer EJ.
Osoegawa K, et al. Among authors: mohammed n.
Mol Genet Genomic Med. 2014 Jul;2(4):341-51. doi: 10.1002/mgg3.75. Epub 2014 Apr 17.
Mol Genet Genomic Med. 2014.
PMID: 25077177
Free PMC article.
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