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Contribution of next generation sequencing in pediatric practice in Lebanon. A Study on 213 cases.
Nair P, Sabbagh S, Mansour H, Fawaz A, Hmaimess G, Noun P, Dagher R, Megarbane H, Hana S, Alame S, Lamaa M, Hasbini D, Farah R, Rajab M, Stora S, El-Tourjuman O, Abou Jaoude P, Chalouhi G, Sayad R, Gillart AC, Al-Ali M, Delague V, El-Hayek S, Mégarbané A. Nair P, et al. Among authors: megarbane h. Mol Genet Genomic Med. 2018 Nov;6(6):1041-1052. doi: 10.1002/mgg3.480. Epub 2018 Oct 7. Mol Genet Genomic Med. 2018. PMID: 30293248 Free PMC article.
Clinical and Molecular Update on the Fourth Reported Family with Hamamy Syndrome.
Mégarbané A, Hana S, Mégarbané H, Castro C, Baulande S, Criqui A, Roëckel-Trevisiol N, Dagher C, Al-Ali MT, Desvignes JP, Mahfoud D, El-Hayek S, Delague V. Mégarbané A, et al. Among authors: megarbane h. Mol Syndromol. 2021 Oct;12(6):342-350. doi: 10.1159/000517253. Epub 2021 Aug 31. Mol Syndromol. 2021. PMID: 34899143 Free PMC article.
[Congenital exfoliative erythroderma].
Mégarbané H, Tomb R, Klein-Tomb L, Mégarbané A. Mégarbané H, et al. Among authors: megarbane a. Ann Dermatol Venereol. 2004 Feb;131(2):211-2. doi: 10.1016/s0151-9638(04)93576-4. Ann Dermatol Venereol. 2004. PMID: 15026755 French. No abstract available.
An autosomal-recessive form of cutis laxa is due to homozygous elastin mutations, and the phenotype may be modified by a heterozygous fibulin 5 polymorphism.
Mégarbané H, Florence J, Sass JO, Schwonbeck S, Foglio M, de Cid R, Cure S, Saker S, Mégarbané A, Fischer J. Mégarbané H, et al. Among authors: megarbane a. J Invest Dermatol. 2009 Jul;129(7):1650-5. doi: 10.1038/jid.2008.450. Epub 2009 Feb 5. J Invest Dermatol. 2009. PMID: 19194475 Free article.
26 results