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Triple-A Syndrome in Morocco: Founder Effect, Age Estimation of the AAAS c.1331+1G>A Variant, and Implications for Genetic Diagnosis.
Belmokhtar KY, Cherkaoui I, Lhousni S, Elidrissi Errahhali M, Elidrissi Errahhali M, Charif M, Boulouiz R, Ouarzane M, Elouali A, Ghanam A, Babakhouya A, Rkain M, Benajiba N, Bellaoui M. Belmokhtar KY, et al. Among authors: ghanam a. Mol Syndromol. 2024 Mar;15(2):96-103. doi: 10.1159/000533894. Epub 2023 Sep 29. Mol Syndromol. 2024. PMID: 38585542
First report on chromosomal abnormalities in Eastern Morocco: Identification of a new case of a de novo partial trisomy 13q using single-nucleotide polymorphism array.
Elidrissi Errahhali M, Elidrissi Errahhali M, Ramdani S, Lhousni S, Benajiba N, Rkain M, Babakhouya A, Elouali A, Ghanam A, Amrani R, Messaoudi S, Ayyad A, Oneib B, Mimouni A, Saadi H, Allaoui S, Ouarzane M, Guichet A, Charif M, Boulouiz R, Bellaoui M. Elidrissi Errahhali M, et al. Among authors: ghanam a. Arch Pediatr. 2024 Feb;31(2):112-116. doi: 10.1016/j.arcped.2023.10.002. Epub 2024 Jan 22. Arch Pediatr. 2024. PMID: 38262863
Generation and Comparative Analysis of an Itga8-CreER T2 Mouse with Preferential Activity in Vascular Smooth Muscle Cells.
Warthi G, Faulkner JL, Doja J, Ghanam AR, Gao P, Yang AC, Slivano OJ, Barris CT, Kress TC, Zawieja SD, Griffin SH, Xie X, Ashworth A, Christie CK, Bryant WB, Kumar A, Davis MJ, Long X, Gan L, Belin de Chantemele EJ, Lyu Q, Miano JM. Warthi G, et al. Among authors: ghanam ar. Nat Cardiovasc Res. 2022 Nov;1(11):1084-1100. doi: 10.1038/s44161-022-00162-1. Epub 2022 Nov 11. Nat Cardiovasc Res. 2022. PMID: 36424917 Free PMC article.
Bean Syndrome in a Child Treated with Sirolimus: About a Case.
Ghanam A, Elouali A, Nour M, Rkain M, Benajiba N, Babakhouya A. Ghanam A, et al. Case Rep Pediatr. 2022 May 24;2022:8245139. doi: 10.1155/2022/8245139. eCollection 2022. Case Rep Pediatr. 2022. PMID: 35656331 Free PMC article.
29 results