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Sushma Singh

Showing results (81-90 of 82) with videos related to

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European Journal of Human Genetics : EJHG|April 18, 2023
Highly variable hearing loss due to POU4F3 (c.37del) is revealed by longitudinal, frequency specific analysesSushma Singh, Cindy Penney, Anne Griffin, et al.
Human Genetics|March 12, 2022
Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase geneJustin A Pater, Cindy Penney, Darren D O'Rielly, et al.
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Showing results (81-90 of 82) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 82 results.
European Journal of Human Genetics : EJHG|April 18, 2023
Highly variable hearing loss due to POU4F3 (c.37del) is revealed by longitudinal, frequency specific analysesSushma Singh, Cindy Penney, Anne Griffin, et al.
Human Genetics|March 12, 2022
Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase geneJustin A Pater, Cindy Penney, Darren D O'Rielly, et al.
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