K. Turki

Identification of candidate regions for a novel Usher syndrome type II locus

M. Vikkula, S. Masmoudi, H. Ayadi, 2008, Molecular vision.

A genome-wide linkage scan in Tunisian families identifies a novel locus for non-syndromic posterior microphthalmia to chromosome 2q37.1

M. Khairallah, P. Söderkvist, A. Rebaï, 2009, Human Genetics.

A novel missense mutation in the ESRRB gene causes DFNB35 hearing loss in a Tunisian family.

S. Masmoudi, H. Ayadi, I. Castillo, 2011, European journal of medical genetics.

Localization of a Novel Autosomal Recessive Non‐syndromic Hearing Impairment Locus DFNB63 to Chromosome 11q13.3‐q13.4

A. Tlili, S. Masmoudi, H. Ayadi, 2007, Annals of human genetics.