Amel Boulila-Elgaied

A novel locus for Usher syndrome type II, USH2B, maps to chromosome 3 at p23–24.2

C. Petit, H. Ayadi, Z. B. Zina, 1999, European Journal of Human Genetics.

Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene.

C. Petit, M. Mustapha, D. Weil, 1997, Human molecular genetics.

Mutations of GJB2 in three geographic isolates from northern Tunisia: evidence for genetic heterogeneity within isolates

C. Petit, S. Chardenoux, F. Denoyelle, 2000, Clinical genetics.