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Human Genomics
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June 25, 2015
Genomics in the renal clinic - translating nephrogenetics for clinical practice
Andrew Mallett, Christopher Corney, Hugh McCarthy, et al.
Human Genomics
|
June 17, 2015
Clinical application of next-generation sequencing for Mendelian diseases
Saumya Shekhar Jamuar, Ene-Choo Tan
Human Genomics
|
June 7, 2020
Clinical performance of non-invasive prenatal served as a first-tier screening test for trisomy 21, 18, 13 and sex chromosome aneuploidy in a pilot city in China
Yanhui Liu, Hailiang Liu, Yi He, et al.
Human Genomics
|
June 12, 2020
Whole-genome sequencing of Chinese centenarians reveals important genetic variants in aging WGS of centenarian for genetic analysis of aging
Shuhua Shen, Chao Li, Luwei Xiao, et al.
Human Genomics
|
November 11, 2022
De novo and inherited variants in coding and regulatory regions in genetic cardiomyopathies
Nirmal Vadgama, Mohamed Ameen, Laksshman Sundaram, et al.
Human Genomics
|
November 12, 2022
Mutation in XPO5 causes adult-onset autosomal dominant familial focal segmental glomerulosclerosis
Hafiz Muhammad Jafar Hussain, Yikai Cai, Qinjie Weng, et al.
Human Genomics
|
July 20, 2006
Genetic factors leading to chronic Epstein-Barr virus infection and nasopharyngeal carcinoma in South East China: study design, methods and feasibility
Xiu Chan Guo, Kevin Scott, Yan Liu, et al.
Human Genomics
|
December 14, 2004
Characterisation of SNP haplotype structure in chemokine and chemokine receptor genes using CEPH pedigrees and statistical estimation
Vanessa J Clark, Michael Dean
Human Genomics
|
December 14, 2004
Human pharmacogenomics: the development of a science
Werner Kalow
Human Genomics
|
December 17, 2004
Genome-wide characterisation of the binding repertoire of small molecule drugs
Lee Makowski, Diane J Rodi
Page
of 125
Search research articles
Search
Showing results (71-80 of 1,248) with videos related to
Sort By:
Page
of 125
Human Genomics
|
June 25, 2015
Genomics in the renal clinic - translating nephrogenetics for clinical practice
Andrew Mallett, Christopher Corney, Hugh McCarthy, et al.
Human Genomics
|
June 17, 2015
Clinical application of next-generation sequencing for Mendelian diseases
Saumya Shekhar Jamuar, Ene-Choo Tan
Human Genomics
|
June 7, 2020
Clinical performance of non-invasive prenatal served as a first-tier screening test for trisomy 21, 18, 13 and sex chromosome aneuploidy in a pilot city in China
Yanhui Liu, Hailiang Liu, Yi He, et al.
Human Genomics
|
June 12, 2020
Whole-genome sequencing of Chinese centenarians reveals important genetic variants in aging WGS of centenarian for genetic analysis of aging
Shuhua Shen, Chao Li, Luwei Xiao, et al.
Human Genomics
|
November 11, 2022
De novo and inherited variants in coding and regulatory regions in genetic cardiomyopathies
Nirmal Vadgama, Mohamed Ameen, Laksshman Sundaram, et al.
Human Genomics
|
November 12, 2022
Mutation in XPO5 causes adult-onset autosomal dominant familial focal segmental glomerulosclerosis
Hafiz Muhammad Jafar Hussain, Yikai Cai, Qinjie Weng, et al.
Human Genomics
|
July 20, 2006
Genetic factors leading to chronic Epstein-Barr virus infection and nasopharyngeal carcinoma in South East China: study design, methods and feasibility
Xiu Chan Guo, Kevin Scott, Yan Liu, et al.
Human Genomics
|
December 14, 2004
Characterisation of SNP haplotype structure in chemokine and chemokine receptor genes using CEPH pedigrees and statistical estimation
Vanessa J Clark, Michael Dean
Human Genomics
|
December 14, 2004
Human pharmacogenomics: the development of a science
Werner Kalow
Human Genomics
|
December 17, 2004
Genome-wide characterisation of the binding repertoire of small molecule drugs
Lee Makowski, Diane J Rodi
Page
of 125