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Orphanet Journal of Rare Diseases
|
May 17, 2011
Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis
Crystel Bonnet, M'hamed Grati, Sandrine Marlin, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 8, 2025
Genetics of prelingual isolated deafness and Usher syndrome in the Maghreb and Jordan: Harnessing the potential of homozygosity
Zied Riahi, Sophie Boucher, Samia Abdi, et al.
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of 8
Search research articles
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Showing results (71-80 of 72) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 72 results.
Orphanet Journal of Rare Diseases
|
May 17, 2011
Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis
Crystel Bonnet, M'hamed Grati, Sandrine Marlin, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 8, 2025
Genetics of prelingual isolated deafness and Usher syndrome in the Maghreb and Jordan: Harnessing the potential of homozygosity
Zied Riahi, Sophie Boucher, Samia Abdi, et al.
Page
of 8