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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 19, 2023
Clinical genome sequencing: Three years' experience at a tertiary children's hospital
Runjun D Kumar, Lisa F Saba, Haley Streff, et al.
American Journal of Human Genetics
|
May 3, 2016
Integrative Multi-omic Analysis of Human Platelet eQTLs Reveals Alternative Start Site in Mitofusin 2
Lukas M Simon, Edward S Chen, Leonard C Edelstein, et al.
Plos Genetics
|
April 5, 2013
Ataxin1L is a regulator of HSC function highlighting the utility of cross-tissue comparisons for gene discovery
Juliette J Kahle, George P Souroullas, Peng Yu, et al.
Plos One
|
March 15, 2014
Gene sequence variability of the three surface proteins of human respiratory syncytial virus (HRSV) in Texas
Lorena I Tapia, Chad A Shaw, Letisha O Aideyan, et al.
European Journal of Human Genetics : EJHG
|
September 5, 2025
Clinical exome sequencing efficacy and phenotypic expansions involving non-isolated congenital anomalies of kidney and urinary tract (CAKUT+)
E Andres Rivera-Munoz, Xiaonan E Zhao, Jill A Rosenfeld, et al.
American Journal of Human Genetics
|
August 19, 2007
Oral curcumin mitigates the clinical and neuropathologic phenotype of the Trembler-J mouse: a potential therapy for inherited neuropathy
Mehrdad Khajavi, Kensuke Shiga, Wojciech Wiszniewski, et al.
Journal of Cellular Physiology
|
May 1, 2008
Brachy-syndactyly caused by loss of Sfrp2 function
Roy Morello, Terry K Bertin, Silke Schlaubitz, et al.
Science (New York, N.Y.)
|
August 15, 2015
DNA REPAIR. Mus81 and converging forks limit the mutagenicity of replication fork breakage
Ryan Mayle, Ian M Campbell, Christine R Beck, et al.
American Journal of Medical Genetics. Part A
|
April 17, 2008
Low-level mosaicism of trisomy 14: phenotypic and molecular characterization
Marwan Shinawi, Lina Shao, Linda Jo Bone Jeng, et al.
BMC Medical Genomics
|
April 24, 2014
Testicular sex cord-stromal tumor in a boy with 2q37 deletion syndrome
Yasunari Sakai, Ryota Souzaki, Hidetaka Yamamoto, et al.
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of 18
Search research articles
Search
Showing results (41-50 of 171) with videos related to
Sort By:
Page
of 18
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 19, 2023
Clinical genome sequencing: Three years' experience at a tertiary children's hospital
Runjun D Kumar, Lisa F Saba, Haley Streff, et al.
American Journal of Human Genetics
|
May 3, 2016
Integrative Multi-omic Analysis of Human Platelet eQTLs Reveals Alternative Start Site in Mitofusin 2
Lukas M Simon, Edward S Chen, Leonard C Edelstein, et al.
Plos Genetics
|
April 5, 2013
Ataxin1L is a regulator of HSC function highlighting the utility of cross-tissue comparisons for gene discovery
Juliette J Kahle, George P Souroullas, Peng Yu, et al.
Plos One
|
March 15, 2014
Gene sequence variability of the three surface proteins of human respiratory syncytial virus (HRSV) in Texas
Lorena I Tapia, Chad A Shaw, Letisha O Aideyan, et al.
European Journal of Human Genetics : EJHG
|
September 5, 2025
Clinical exome sequencing efficacy and phenotypic expansions involving non-isolated congenital anomalies of kidney and urinary tract (CAKUT+)
E Andres Rivera-Munoz, Xiaonan E Zhao, Jill A Rosenfeld, et al.
American Journal of Human Genetics
|
August 19, 2007
Oral curcumin mitigates the clinical and neuropathologic phenotype of the Trembler-J mouse: a potential therapy for inherited neuropathy
Mehrdad Khajavi, Kensuke Shiga, Wojciech Wiszniewski, et al.
Journal of Cellular Physiology
|
May 1, 2008
Brachy-syndactyly caused by loss of Sfrp2 function
Roy Morello, Terry K Bertin, Silke Schlaubitz, et al.
Science (New York, N.Y.)
|
August 15, 2015
DNA REPAIR. Mus81 and converging forks limit the mutagenicity of replication fork breakage
Ryan Mayle, Ian M Campbell, Christine R Beck, et al.
American Journal of Medical Genetics. Part A
|
April 17, 2008
Low-level mosaicism of trisomy 14: phenotypic and molecular characterization
Marwan Shinawi, Lina Shao, Linda Jo Bone Jeng, et al.
BMC Medical Genomics
|
April 24, 2014
Testicular sex cord-stromal tumor in a boy with 2q37 deletion syndrome
Yasunari Sakai, Ryota Souzaki, Hidetaka Yamamoto, et al.
Page
of 18