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Biomed Research International
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June 21, 2017
An Integrative Developmental Genomics and Systems Biology Approach to Identify an In Vivo Sox Trio-Mediated Gene Regulatory Network in Murine Embryos
Wenqing Jean Lee, Sumantra Chatterjee, Sook Peng Yap, et al.
The New England Journal of Medicine
|
April 11, 2019
Molecular Genetic Anatomy and Risk Profile of Hirschsprung's Disease
Joseph M Tilghman, Albee Y Ling, Tychele N Turner, et al.
European Journal of Human Genetics : EJHG
|
January 31, 2018
Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus
João Fadista, Marie Lund, Line Skotte, et al.
American Journal of Human Genetics
|
May 27, 2014
An enhancer polymorphism at the cardiomyocyte intercalated disc protein NOS1AP locus is a major regulator of the QT interval
Ashish Kapoor, Rajesh B Sekar, Nancy F Hansen, et al.
Human Genomics
|
July 14, 2021
Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism
Evin M Padhi, Tristan J Hayeck, Zhang Cheng, et al.
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of 4
Search research articles
Search
Showing results (31-40 of 35) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 35 results.
Biomed Research International
|
June 21, 2017
An Integrative Developmental Genomics and Systems Biology Approach to Identify an In Vivo Sox Trio-Mediated Gene Regulatory Network in Murine Embryos
Wenqing Jean Lee, Sumantra Chatterjee, Sook Peng Yap, et al.
The New England Journal of Medicine
|
April 11, 2019
Molecular Genetic Anatomy and Risk Profile of Hirschsprung's Disease
Joseph M Tilghman, Albee Y Ling, Tychele N Turner, et al.
European Journal of Human Genetics : EJHG
|
January 31, 2018
Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus
João Fadista, Marie Lund, Line Skotte, et al.
American Journal of Human Genetics
|
May 27, 2014
An enhancer polymorphism at the cardiomyocyte intercalated disc protein NOS1AP locus is a major regulator of the QT interval
Ashish Kapoor, Rajesh B Sekar, Nancy F Hansen, et al.
Human Genomics
|
July 14, 2021
Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism
Evin M Padhi, Tristan J Hayeck, Zhang Cheng, et al.
Page
of 4