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Simone Khalifeh

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Le Journal Medical Libanais. the Lebanese Medical Journal|November 20, 2018
AUTISM IN REVIEWSimone Khalifeh, Walid Yassin, Silva Kourtian, et al.
Clinical Case Reports|February 2, 2026
Rare DMD Gene Duplication in a Lebanese Child With Duchene Muscular DystrophyNada Assaf, Jeanette El Hajj, Jana Doghman, et al.
BMC Medical Genomics|December 19, 2025
Novel TRIP12 variants in two Lebanese patients with neurodevelopmental delaySimone Khalifeh, Nadine J Makhoul, Samah Trad, et al.
American Journal of Human Genetics|April 11, 2025
FBXO22 deficiency defines a pleiotropic syndrome of growth restriction and multi-system anomalies associated with a unique epigenetic signatureNavin B Ramakrishna, Umar Bin Mohamad Sahari, Yoshikazu Johmura, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Le Journal Medical Libanais. the Lebanese Medical Journal|November 20, 2018
AUTISM IN REVIEWSimone Khalifeh, Walid Yassin, Silva Kourtian, et al.
Clinical Case Reports|February 2, 2026
Rare DMD Gene Duplication in a Lebanese Child With Duchene Muscular DystrophyNada Assaf, Jeanette El Hajj, Jana Doghman, et al.
BMC Medical Genomics|December 19, 2025
Novel TRIP12 variants in two Lebanese patients with neurodevelopmental delaySimone Khalifeh, Nadine J Makhoul, Samah Trad, et al.
American Journal of Human Genetics|April 11, 2025
FBXO22 deficiency defines a pleiotropic syndrome of growth restriction and multi-system anomalies associated with a unique epigenetic signatureNavin B Ramakrishna, Umar Bin Mohamad Sahari, Yoshikazu Johmura, et al.
Pageof 1