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Year | Number of Results |
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2011 | 2 |
2017 | 1 |
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Page 1
Exploring Muslims' Health-Related Behaviours in Portugal: Any Impact on Quotidian Community Pharmacy Practice?
Pharmacy (Basel). 2022 May 20;10(3):55. doi: 10.3390/pharmacy10030055.
Pharmacy (Basel). 2022.
PMID: 35645334
Free PMC article.
Whole exome sequencing in ADHD trios from single and multi-incident families implicates new candidate genes and highlights polygenic transmission.
Al-Mubarak BR, Omar A, Baz B, Al-Abdulaziz B, Magrashi AI, Al-Yemni E, Jabaan A, Monies D, Abouelhoda M, Abebe D, Ghaziuddin M, Al-Tassan NA.
Al-Mubarak BR, et al. Among authors: omar a.
Eur J Hum Genet. 2020 Aug;28(8):1098-1110. doi: 10.1038/s41431-020-0619-7. Epub 2020 Apr 1.
Eur J Hum Genet. 2020.
PMID: 32238911
Free PMC article.
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Obesity epidemic in urban Tanzania: a public health calamity in an already overwhelmed and fragmented health system.
Pallangyo P, Mkojera ZS, Hemed NR, Swai HJ, Misidai N, Mgopa L, Bhalia S, Millinga J, Mushi TL, Kabeya L, Omar A, Kaijage A, Mulashani R, Mosha S, Mwapinga F, Janabi M.
Pallangyo P, et al. Among authors: omar a.
BMC Endocr Disord. 2020 Sep 29;20(1):147. doi: 10.1186/s12902-020-00631-3.
BMC Endocr Disord. 2020.
PMID: 32993615
Free PMC article.
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The optic nerve head in congenital fibrosis of the extraocular muscles.
Khan AO, Shinwari J, Omar A, Khalil D, Al-Anazi M, Al-Amri A, Al-Tassan NA.
Khan AO, et al. Among authors: omar a.
Ophthalmic Genet. 2011 Sep;32(3):175-80. doi: 10.3109/13816810.2011.567318. Epub 2011 Mar 31.
Ophthalmic Genet. 2011.
PMID: 21449832
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Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families.
Al-Mubarak B, Abouelhoda M, Omar A, AlDhalaan H, Aldosari M, Nester M, Alshamrani HA, El-Kalioby M, Goljan E, Albar R, Subhani S, Tahir A, Asfahani S, Eskandrani A, Almusaiab A, Magrashi A, Shinwari J, Monies D, Al Tassan N.
Al-Mubarak B, et al. Among authors: omar a.
Sci Rep. 2017 Jul 18;7(1):5679. doi: 10.1038/s41598-017-06033-1.
Sci Rep. 2017.
PMID: 28720891
Free PMC article.
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Lack of KIF21A mutations in congenital fibrosis of the extraocular muscles type I patients from consanguineous Saudi Arabian families.
Khan AO, Shinwari J, Omar A, Al-Sharif L, Khalil DS, Alanazi M, Al-Amri A, Al Tassan N.
Khan AO, et al. Among authors: omar a.
Mol Vis. 2011 Jan 20;17:218-24.
Mol Vis. 2011.
PMID: 21264235
Free PMC article.
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