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Shirley Henderson

Showing results (11-20 of 22) with videos related to

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European Journal of Human Genetics : EJHG|July 24, 2014
EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathiesJoanne Traeger-Synodinos, Cornelis L Harteveld, John M Old, et al.
Genetic Testing and Molecular Biomarkers|August 21, 2010
Neonatal screening for hemoglobinopathies: results of a public health system in South BrazilSandrine C Wagner, Simone M de Castro, Tatiana P Gonzalez, et al.
Frontiers in Oncology|May 21, 2016
Durable Response of Spinal Chordoma to Combined Inhibition of IGF-1R and EGFRTamara Aleksic, Lisa Browning, Martha Woodward, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 5, 2009
Adventitious changes in long-range gene expression caused by polymorphic structural variation and promoter competitionKaren M Lower, Jim R Hughes, Marco De Gobbi, et al.
Plos One|September 15, 2016
Targeted Next-Generation Sequencing of Plasma DNA from Cancer Patients: Factors Influencing Consistency with Tumour DNA and Prospective Investigation of Its Utility for DiagnosisPamela J Kaisaki, Anthony Cutts, Niko Popitsch, et al.
Plos Medicine|February 15, 2017
Clinical applicability and cost of a 46-gene panel for genomic analysis of solid tumours: Retrospective validation and prospective audit in the UK National Health ServiceAngela Hamblin, Sarah Wordsworth, Jilles M Fermont, et al.
Blood|August 24, 2012
Monitoring chronic lymphocytic leukemia progression by whole genome sequencing reveals heterogeneous clonal evolution patternsAnna Schuh, Jennifer Becq, Sean Humphray, et al.
Blood|March 29, 2013
Impact of isolated germline JAK2V617I mutation on human hematopoiesisAdam J Mead, Onima Chowdhury, Christian Pecquet, et al.
Virchows Archiv : an International Journal of Pathology|September 29, 2016
Integration of next-generation sequencing in clinical diagnostic molecular pathology laboratories for analysis of solid tumours; an expert opinion on behalf of IQN Path ASBLZandra C Deans, Jose Luis Costa, Ian Cree, et al.
British Journal of Haematology|July 20, 2016
A novel 33-Gene targeted resequencing panel provides accurate, clinical-grade diagnosis and improves patient management for rare inherited anaemiasNoémi B A Roy, Edward A Wilson, Shirley Henderson, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
European Journal of Human Genetics : EJHG|July 24, 2014
EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathiesJoanne Traeger-Synodinos, Cornelis L Harteveld, John M Old, et al.
Genetic Testing and Molecular Biomarkers|August 21, 2010
Neonatal screening for hemoglobinopathies: results of a public health system in South BrazilSandrine C Wagner, Simone M de Castro, Tatiana P Gonzalez, et al.
Frontiers in Oncology|May 21, 2016
Durable Response of Spinal Chordoma to Combined Inhibition of IGF-1R and EGFRTamara Aleksic, Lisa Browning, Martha Woodward, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 5, 2009
Adventitious changes in long-range gene expression caused by polymorphic structural variation and promoter competitionKaren M Lower, Jim R Hughes, Marco De Gobbi, et al.
Plos One|September 15, 2016
Targeted Next-Generation Sequencing of Plasma DNA from Cancer Patients: Factors Influencing Consistency with Tumour DNA and Prospective Investigation of Its Utility for DiagnosisPamela J Kaisaki, Anthony Cutts, Niko Popitsch, et al.
Plos Medicine|February 15, 2017
Clinical applicability and cost of a 46-gene panel for genomic analysis of solid tumours: Retrospective validation and prospective audit in the UK National Health ServiceAngela Hamblin, Sarah Wordsworth, Jilles M Fermont, et al.
Blood|August 24, 2012
Monitoring chronic lymphocytic leukemia progression by whole genome sequencing reveals heterogeneous clonal evolution patternsAnna Schuh, Jennifer Becq, Sean Humphray, et al.
Blood|March 29, 2013
Impact of isolated germline JAK2V617I mutation on human hematopoiesisAdam J Mead, Onima Chowdhury, Christian Pecquet, et al.
Virchows Archiv : an International Journal of Pathology|September 29, 2016
Integration of next-generation sequencing in clinical diagnostic molecular pathology laboratories for analysis of solid tumours; an expert opinion on behalf of IQN Path ASBLZandra C Deans, Jose Luis Costa, Ian Cree, et al.
British Journal of Haematology|July 20, 2016
A novel 33-Gene targeted resequencing panel provides accurate, clinical-grade diagnosis and improves patient management for rare inherited anaemiasNoémi B A Roy, Edward A Wilson, Shirley Henderson, et al.
Pageof 3