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Epigenomes
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April 24, 2026
Novel Perspectives on <i>ATP8A2</i> Regulation: Evidence for Parental Imprinting and Chimeric Transcript Formation
Abdelhamid 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 review
Amal 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 CADASIL
Amal 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 men
Saadia Amasdl, Said Trhanint, Mohamed Ahakoud, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 4) with videos related to
Sort By:
Page
of 1
Epigenomes
|
April 24, 2026
Novel Perspectives on <i>ATP8A2</i> Regulation: Evidence for Parental Imprinting and Chimeric Transcript Formation
Abdelhamid 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 review
Amal 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 CADASIL
Amal 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 men
Saadia Amasdl, Said Trhanint, Mohamed Ahakoud, et al.
Page
of 1