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Carla Nishimura

Showing results (21-30 of 23) with videos related to

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Journal of the American Society of Nephrology : JASN|August 19, 2015
High-Throughput Genetic Testing for Thrombotic Microangiopathies and C3 GlomerulopathiesFengxiao Bu, Nicolo Ghiringhelli Borsa, Michael B Jones, et al.
International Journal of Pediatric Otorhinolaryngology|June 15, 2012
The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss--a twelve year studyNiloofar Bazazzadegan, Nooshin Nikzat, Zohreh Fattahi, et al.
European Journal of Human Genetics : EJHG|January 5, 2021
A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicingYoel Hirsch, Chayada Tangshewinsirikul, Kevin T Booth, et al.
Pageof 3

Showing results (21-30 of 23) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 23 results.
Journal of the American Society of Nephrology : JASN|August 19, 2015
High-Throughput Genetic Testing for Thrombotic Microangiopathies and C3 GlomerulopathiesFengxiao Bu, Nicolo Ghiringhelli Borsa, Michael B Jones, et al.
International Journal of Pediatric Otorhinolaryngology|June 15, 2012
The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss--a twelve year studyNiloofar Bazazzadegan, Nooshin Nikzat, Zohreh Fattahi, et al.
European Journal of Human Genetics : EJHG|January 5, 2021
A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicingYoel Hirsch, Chayada Tangshewinsirikul, Kevin T Booth, et al.
Pageof 3