Publications by authors named "Simone Khalifeh"

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Novel TRIP12 variants in two Lebanese patients with neurodevelopmental delay.
Simone Khalifeh, Nadine J Makhoul, Samah Trad, Sara Amro, Medhat Siddik

BMC Med Genomics· December 2025

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FBXO22 deficiency defines a pleiotropic syndrome of growth restriction and multi-system anomalies associated with a unique epigenetic signature.
Navin B Ramakrishna, Umar Bin Mohamad Sahari, Yoshikazu Johmura, Nur Ain Ali, Malak Alghamdi, Simone Khalifeh

Am J Hum Genet· May 2025

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AUTISM IN REVIEW.
Simone Khalifeh, Walid Yassin, Silva Kourtian, Rose-Mary Boustany

J Med Liban· August 2016

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