Ikhlas Ben Ayed

Years Active: 2021-2022
Publications (10 Years): 3

This page only lists publications with an associated author ORCID identifier.

Publications

Mariem Ben Said, Ikhlas Ben Ayed, Ines Elloumi, Mehdi Hasnaoui, Amal Souissi, Nabil Idriss, Hajer Aloulou, Imen Chabchoub, Bayen Maâlej, Dorra Driss, Saber Masmoudi
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. Molecular genetics & genomic medicine 10 (2) (2022)
Ikhlas Ben Ayed, Amal Bouzid, Fatma Kammoun, Amal Souissi, Olfa Jallouli, Salma Mallouli, Souhir Guidara, Salma Loukil, Hajer Aloulou, Fida Jbeli, Sahar Aouichaoui, Dorra Abid, Fatma Abdelhedi, Chahnez Triki, Hassen Kamoun, Saber Masmoudi
8q21.11 microdeletion syndrome: Delineation of HEY1 as a candidate gene in neurodevelopmental and cardiac defects. Molecular genetics & genomic medicine 9 (11) (2021)
Ikhlas Ben Ayed, Wael Ouarda, Fakher Frikha, Fatma Kammoun, Amal Souissi, Mariem Ben Said, Amal Bouzid, Ines Elloumi, Tarak M Hamdani, Nourhene Gharbi, Nesrine Baklouti, Manel Guirat, Fatma Mejdoub, Najla Kharrat, Imene Boujelbene, Fatma Abdelhedi, Neila Belguith, Leila Keskes, Abdullah Ahmed Gibriel, Hassen Kamoun, Chahnez Triki, Adel M Alimi, Saber Masmoudi
SRD5A3-CDG: 3D structure modeling, clinical spectrum, and computer-based dysmorphic facial recognition. American journal of medical genetics. Part A 185 (4) (2021)

Ikhlas Ben Ayed.css-eqlu8i{font-size:small;padding-left:4px;}