HuGE Literature Finder
Records 1-3
Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss.
PloS one 2015 10 (11): e0142154. Atik Tahir, Onay Huseyin, Aykut Ayca, Bademci Guney, Kirazli Tayfun, Tekin Mustafa, Ozkinay Fer |
Targeted next generation sequencing for molecular diagnosis of Usher syndrome.
Orphanet journal of rare diseases 2014 9 168. Aparisi María J, Aller Elena, Fuster-García Carla, García-García Gema, Rodrigo Regina, Vázquez-Manrique Rafael P, Blanco-Kelly Fiona, Ayuso Carmen, Roux Anne-Françoise, Jaijo Teresa, Millán José |
Sequence variants of the DFNB31 gene among Usher syndrome patients of diverse origin.
Molecular vision 2010 16 495-500. Aller Elena, Jaijo Teresa, van Wijk Erwin, Ebermann Inga, Kersten Ferry, García-García Gema, Voesenek Krysta, Aparisi María José, Hoefsloot Lies, Cremers Cor, Díaz-Llopis Manuel, Pennings Ronald, Bolz Hanno J, Kremer Hannie, Millán José |
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