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Muhammad Qasim

Showing results (761-770 of 765) with videos related to

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Genetic Epidemiology|November 10, 2022
Multivariate analysis of a missense variant in CREBRF reveals associations with measures of adiposity in people of Polynesian ancestriesJerry Z Zhang, Lacey W Heinsberg, Mohanraj Krishnan, et al.
Journal of Medical Genetics|September 24, 2011
Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotesJulie M Schultz, Rashid Bhatti, Anne C Madeo, et al.
HGG Advances|November 7, 2022
A stop-gain variant in <i>BTNL9</i> is associated with atherogenic lipid profilesJenna C Carlson, Mohanraj Krishnan, Samantha L Rosenthal, et al.
BMC Medical Genetics|June 25, 2015
Novel VPS13B Mutations in Three Large Pakistani Cohen Syndrome Families Suggests a Baloch Variant with Autistic-Like FeaturesMuhammad Arshad Rafiq, Claire S Leblond, Muhammad Arif Nadeem Saqib, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|October 25, 2022
Association of Gout Polygenic Risk Score With Age at Disease Onset and Tophaceous Disease in European and Polynesian Men With GoutNicholas A Sumpter, Riku Takei, Murray Cadzow, et al.
Pageof 77

Showing results (761-770 of 765) with videos related to

Sort By:
Pageof 77
You have reached the last page of results.This site can display upto 765 results.
Genetic Epidemiology|November 10, 2022
Multivariate analysis of a missense variant in CREBRF reveals associations with measures of adiposity in people of Polynesian ancestriesJerry Z Zhang, Lacey W Heinsberg, Mohanraj Krishnan, et al.
Journal of Medical Genetics|September 24, 2011
Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotesJulie M Schultz, Rashid Bhatti, Anne C Madeo, et al.
HGG Advances|November 7, 2022
A stop-gain variant in <i>BTNL9</i> is associated with atherogenic lipid profilesJenna C Carlson, Mohanraj Krishnan, Samantha L Rosenthal, et al.
BMC Medical Genetics|June 25, 2015
Novel VPS13B Mutations in Three Large Pakistani Cohen Syndrome Families Suggests a Baloch Variant with Autistic-Like FeaturesMuhammad Arshad Rafiq, Claire S Leblond, Muhammad Arif Nadeem Saqib, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|October 25, 2022
Association of Gout Polygenic Risk Score With Age at Disease Onset and Tophaceous Disease in European and Polynesian Men With GoutNicholas A Sumpter, Riku Takei, Murray Cadzow, et al.
Pageof 77