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La Tunisie Medicale
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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, harmonin
Dominique 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 1p13.3-22.1
Saber Masmoudi, Abdelaziz Tlili, Marja Majava, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 4) with videos related to
Sort By:
Page
of 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, harmonin
Dominique 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 1p13.3-22.1
Saber Masmoudi, Abdelaziz Tlili, Marja Majava, et al.
Page
of 1