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Amal Ouskri

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

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Epigenomes|April 24, 2026
Novel Perspectives on <i>ATP8A2</i> Regulation: Evidence for Parental Imprinting and Chimeric Transcript FormationAbdelhamid Bouramtane, Badreddine Elmakhzen, Amal Ouskri, et al.
Clinical Dysmorphology|November 6, 2025
A rare case of mosaic monosomy 21 in a Moroccan patient: clinical findings and insights from a systematic reviewAmal Ouskri, Abdelhamid Bouramtane, Rania Bouchikhi, et al.
Neurogenetics|November 6, 2025
A novel homozygous loss-of-function NOTCH3 variant in a Moroccan patient: expanding the spectrum beyond CADASILAmal Ouskri, Hajar Ihlal, Zaid En-Nasery, et al.
Clinical and Experimental Reproductive Medicine|May 7, 2026
Prevalence and spectrum of AZFc copy number variations in infertile Moroccan menSaadia Amasdl, Said Trhanint, Mohamed Ahakoud, et al.
Pageof 1

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

Sort By:
Pageof 1
Epigenomes|April 24, 2026
Novel Perspectives on <i>ATP8A2</i> Regulation: Evidence for Parental Imprinting and Chimeric Transcript FormationAbdelhamid Bouramtane, Badreddine Elmakhzen, Amal Ouskri, et al.
Clinical Dysmorphology|November 6, 2025
A rare case of mosaic monosomy 21 in a Moroccan patient: clinical findings and insights from a systematic reviewAmal Ouskri, Abdelhamid Bouramtane, Rania Bouchikhi, et al.
Neurogenetics|November 6, 2025
A novel homozygous loss-of-function NOTCH3 variant in a Moroccan patient: expanding the spectrum beyond CADASILAmal Ouskri, Hajar Ihlal, Zaid En-Nasery, et al.
Clinical and Experimental Reproductive Medicine|May 7, 2026
Prevalence and spectrum of AZFc copy number variations in infertile Moroccan menSaadia Amasdl, Said Trhanint, Mohamed Ahakoud, et al.
Pageof 1