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Year | Number of Results |
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2020 | 2 |
2021 | 2 |
2022 | 1 |
2023 | 1 |
2024 | 0 |
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Page 1
A 20-year Clinical and Genetic Neuromuscular Cohort Analysis in Lebanon: An International Effort.
J Neuromuscul Dis. 2022;9(1):193-210. doi: 10.3233/JND-210652.
J Neuromuscul Dis. 2022.
PMID: 34602496
Free PMC article.
Catalogue for Transmission Genetics in Arabs (CTGA) Database: Analysing Lebanese Data on Genetic Disorders.
Bizzari S, Nair P, Deepthi A, Hana S, Al-Ali MT, Megarbané A, El-Hayek S.
Bizzari S, et al. Among authors: deepthi a.
Genes (Basel). 2021 Sep 27;12(10):1518. doi: 10.3390/genes12101518.
Genes (Basel). 2021.
PMID: 34680914
Free PMC article.
Review.
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SIX6-related anophthalmia/microphthalmia: second report on a deletion in a consanguineous family.
Deepthi A, Fakhoury O, Daher M, Gambarini A, El-Hayek S, Megarbane A.
Deepthi A, et al.
Ophthalmic Genet. 2021 Feb;42(1):88-91. doi: 10.1080/13816810.2020.1836660. Epub 2020 Oct 28.
Ophthalmic Genet. 2021.
PMID: 33108933
No abstract available.
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Spectrum of genetic disorders and gene variants in the United Arab Emirates national population: insights from the CTGA database.
Bizzari S, Nair P, Hana S, Deepthi A, Al-Ali MT, Al-Gazali L, El-Hayek S.
Bizzari S, et al. Among authors: deepthi a.
Front Genet. 2023 May 4;14:1177204. doi: 10.3389/fgene.2023.1177204. eCollection 2023.
Front Genet. 2023.
PMID: 37214420
Free PMC article.
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Homozygous deletion of exons 2-7 within TGFB3 gene in a child with severe Loeys-Dietz syndrome and Marfan-like features.
Mégarbané A, Deepthi A, Obeid M, T Al-Ali M, Gambarini A, El-Hayek S.
Mégarbané A, et al. Among authors: deepthi a.
Am J Med Genet A. 2020 May;182(5):1230-1235. doi: 10.1002/ajmg.a.61508. Epub 2020 Feb 5.
Am J Med Genet A. 2020.
PMID: 32022420
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