Ikhlas Ben Ayed

3PUBLICATIONS
1CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)
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Publications (3)

|Jan 08, 2022
Custom Next-Generation Sequencing Identifies Novel Mutations Expanding the Molecular and clinical spectrum of isolated Hearing Impairment or along with defects of the retina, the thyroid, and the kidneys.

Mariem Ben Said, Ikhlas Ben Ayed, Ines Elloumi

|Sep 22, 2021
8q21.11 microdeletion syndrome: Delineation of HEY1 as a candidate gene in neurodevelopmental and cardiac defects.

Ikhlas Ben Ayed, Amal Bouzid, Fatma Kammoun

|Jan 06, 2021
SRD5A3-CDG: 3D structure modeling, clinical spectrum, and computer-based dysmorphic facial recognition.

Ikhlas Ben Ayed, Wael Ouarda, Fakher Frikha

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Frequent Collaborators

1 joint publications

Mariem Ben Said