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Human Mutation
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June 8, 2021
Genome sequencing in congenital cataracts improves diagnostic yield
Alan Ma, John R Grigg, Maree Flaherty, et al.
Elife
|
February 7, 2018
Mitochondrial CoQ deficiency is a common driver of mitochondrial oxidants and insulin resistance
Daniel J Fazakerley, Rima Chaudhuri, Pengyi Yang, et al.
Lancet (London, England)
|
February 14, 2012
Inheritance of coronary artery disease in men: an analysis of the role of the Y chromosome
Fadi J Charchar, Lisa Ds Bloomer, Timothy A Barnes, et al.
Neurology
|
February 11, 2021
Diagnostic Yield of Whole Genome Sequencing After Nondiagnostic Exome Sequencing or Gene Panel in Developmental and Epileptic Encephalopathies
Elizabeth Emma Palmer, Rani Sachdev, Rebecca Macintosh, et al.
Scientific Reports
|
November 21, 2019
Development and validation of a targeted gene sequencing panel for application to disparate cancers
Mark J McCabe, Marie-Emilie A Gauthier, Chia-Ling Chan, et al.
Breast Cancer Research : BCR
|
June 13, 2020
Proteogenomic analysis of Inhibitor of Differentiation 4 (ID4) in basal-like breast cancer
Laura A Baker, Holly Holliday, Daniel Roden, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 6, 2020
Revealing hidden genetic diagnoses in the ocular anterior segment disorders
Alan Ma, Saira Yousoof, John R Grigg, et al.
Brain : a Journal of Neurology
|
October 13, 2018
Brain and retinal atrophy in African-Americans versus Caucasian-Americans with multiple sclerosis: a longitudinal study
Natalia Gonzalez Caldito, Shiv Saidha, Elias S Sotirchos, et al.
Cancer Research Communications
|
March 16, 2023
Potent Stimulation of the Androgen Receptor Instigates a Viral Mimicry Response in Prostate Cancer
Mohammadreza Alizadeh-Ghodsi, Katie L Owen, Scott L Townley, et al.
Parkinsonism & Related Disorders
|
November 16, 2019
Whole genome sequencing for the genetic diagnosis of heterogenous dystonia phenotypes
Kishore R Kumar, Ryan L Davis, Michel C Tchan, et al.
Page
of 49
Search research articles
Search
Showing results (441-450 of 489) with videos related to
Sort By:
Page
of 49
Human Mutation
|
June 8, 2021
Genome sequencing in congenital cataracts improves diagnostic yield
Alan Ma, John R Grigg, Maree Flaherty, et al.
Elife
|
February 7, 2018
Mitochondrial CoQ deficiency is a common driver of mitochondrial oxidants and insulin resistance
Daniel J Fazakerley, Rima Chaudhuri, Pengyi Yang, et al.
Lancet (London, England)
|
February 14, 2012
Inheritance of coronary artery disease in men: an analysis of the role of the Y chromosome
Fadi J Charchar, Lisa Ds Bloomer, Timothy A Barnes, et al.
Neurology
|
February 11, 2021
Diagnostic Yield of Whole Genome Sequencing After Nondiagnostic Exome Sequencing or Gene Panel in Developmental and Epileptic Encephalopathies
Elizabeth Emma Palmer, Rani Sachdev, Rebecca Macintosh, et al.
Scientific Reports
|
November 21, 2019
Development and validation of a targeted gene sequencing panel for application to disparate cancers
Mark J McCabe, Marie-Emilie A Gauthier, Chia-Ling Chan, et al.
Breast Cancer Research : BCR
|
June 13, 2020
Proteogenomic analysis of Inhibitor of Differentiation 4 (ID4) in basal-like breast cancer
Laura A Baker, Holly Holliday, Daniel Roden, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 6, 2020
Revealing hidden genetic diagnoses in the ocular anterior segment disorders
Alan Ma, Saira Yousoof, John R Grigg, et al.
Brain : a Journal of Neurology
|
October 13, 2018
Brain and retinal atrophy in African-Americans versus Caucasian-Americans with multiple sclerosis: a longitudinal study
Natalia Gonzalez Caldito, Shiv Saidha, Elias S Sotirchos, et al.
Cancer Research Communications
|
March 16, 2023
Potent Stimulation of the Androgen Receptor Instigates a Viral Mimicry Response in Prostate Cancer
Mohammadreza Alizadeh-Ghodsi, Katie L Owen, Scott L Townley, et al.
Parkinsonism & Related Disorders
|
November 16, 2019
Whole genome sequencing for the genetic diagnosis of heterogenous dystonia phenotypes
Kishore R Kumar, Ryan L Davis, Michel C Tchan, et al.
Page
of 49