A. Tajouri

In vitro functional characterization of the novel DHH mutations p.(Asn337Lysfs*24) and p.(Glu212Lys) associated with gonadal dysgenesis

F. Kaiser, O. Hiort, M. Kharrat, 2018, Human mutation.

Functional Analysis of Mutations at Codon 127 of the SRY Gene Associated with 46,XY Complete Gonadal Dysgenesis

F. Poulat, M. Kharrat, R. M’rad, 2017, Sexual Development.

Identification of two additional novel mutations in the AR gene associated with severe forms of androgen insensitivity syndrome

H. Chaabouni, M. Kharrat, R. M’rad, 2019, Steroids.

A Novel Nonsense Mutation p.L9X in the SRY Gene Causes Complete Gonadal Dysgenesis in a 46,XY Female Patient

L. B. Jemaa, H. Chaabouni, M. Kharrat, 2016 .

New methodology for repetitive sequences identification in human X and Y chromosomes

Zied Lachiri, Rabeb Touati, Afef Elloumi Oueslati, 2020, Biomedical Signal Processing and Control.

In vitro functional characterization of androgen receptor gene mutations at arginine p.856 of the ligand-binding-domain associated with androgen insensitivity syndrome

O. Hiort, M. Kharrat, R. Werner, 2021, The Journal of Steroid Biochemistry and Molecular Biology.