Associated Papers
Whole-exome sequencing reveals novel genetic variants associated with diverse phenotypes of melanoma cells.
Hartman ML et al.
Molecular Carcinogenesis, 2019
Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss.
Bakhchane A et al.
Plos One, 2017
28472130 (PubMed )
Supplement: pone.0176516.s002.xlsx › Feuil1
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