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Zeineb Ben Zina

Showing results (1-10 of 4) with videos related to

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La Tunisie Medicale|April 3, 2024
Mohamed Slim Werda, Fatma Cheikhrouhou, Zeineb Ben Zina, et al.
Presse Medicale (Paris, France : 1983)|May 20, 2006
[Ophthalmic manifestations of lipoid proteinosis]Dorra Sellami, Abderrahmen Masmoudi, Hamida Turki, et al.
Human Molecular Genetics|February 18, 2003
Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmoninDominique Weil, Aziz El-Amraoui, Saber Masmoudi, et al.
European Journal of Human Genetics : EJHG|March 14, 2003
Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1Saber Masmoudi, Abdelaziz Tlili, Marja Majava, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
La Tunisie Medicale|April 3, 2024
Mohamed Slim Werda, Fatma Cheikhrouhou, Zeineb Ben Zina, et al.
Presse Medicale (Paris, France : 1983)|May 20, 2006
[Ophthalmic manifestations of lipoid proteinosis]Dorra Sellami, Abderrahmen Masmoudi, Hamida Turki, et al.
Human Molecular Genetics|February 18, 2003
Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmoninDominique Weil, Aziz El-Amraoui, Saber Masmoudi, et al.
European Journal of Human Genetics : EJHG|March 14, 2003
Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1Saber Masmoudi, Abdelaziz Tlili, Marja Majava, et al.
Pageof 1