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Gauhar Rehman

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Genes|February 25, 2023
Novel Variants in <i>MPV17, PRX, GJB1</i>, and <i>SACS</i> Cause Charcot-Marie-Tooth and Spastic Ataxia of Charlevoix-Saguenay Type DiseasesQaiser Zaman, Muhammad Abbas Khan, Kalsoom Sahar, et al.
Gene|November 13, 2023
Unveiling genetics of non-syndromic albinism using whole exome sequencing: A comprehensive study of TYR, TYRP1, OCA2 and MC1R genes in 17 familiesQaiser Zaman, Jamshid Khan, Mashal Ahmad, et al.
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Showing results (41-50 of 42) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 42 results.
Genes|February 25, 2023
Novel Variants in <i>MPV17, PRX, GJB1</i>, and <i>SACS</i> Cause Charcot-Marie-Tooth and Spastic Ataxia of Charlevoix-Saguenay Type DiseasesQaiser Zaman, Muhammad Abbas Khan, Kalsoom Sahar, et al.
Gene|November 13, 2023
Unveiling genetics of non-syndromic albinism using whole exome sequencing: A comprehensive study of TYR, TYRP1, OCA2 and MC1R genes in 17 familiesQaiser Zaman, Jamshid Khan, Mashal Ahmad, et al.
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