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Ruth N MacKinnon

Showing results (1-10 of 19) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|March 23, 2018
Analysis of Chromothripsis by Combined FISH and Microarray AnalysisRuth N MacKinnon
Methods in Molecular Biology (Clifton, N.J.)|March 25, 2011
The use of M-FISH and M-BAND to define chromosome abnormalitiesRuth N Mackinnon, Ilse Chudoba
Genetics Research International|May 9, 2012
The role of dicentric chromosome formation and secondary centromere deletion in the evolution of myeloid malignancyRuth N Mackinnon, Lynda J Campbell
Cancer Genetics and Cytogenetics|December 13, 2005
A comparison of two contrasting recurrent isochromosomes 20 found in myelodysplastic syndromes suggests that retention of proximal 20q is a significant factor in myeloid malignanciesRuth N MacKinnon, Lynda J Campbell
Cancer Genetics|August 6, 2013
Chromothripsis under the microscope: a cytogenetic perspective of two cases of AML with catastrophic chromosome rearrangementRuth N Mackinnon, Lynda J Campbell
Cancer Genetics and Cytogenetics|August 17, 2005
Recurrent duplication of Xq27-qter in hematological malignancies revealed by multicolor fluorescence in situ hybridization and multicolor bandingRuth N MacKinnon, Adrian Zordan, Lynda J Campbell
Molecular Cytogenetics|March 25, 2016
Active centromere and chromosome identification in fixed cell linesThian T Beh, Ruth N MacKinnon, Paul Kalitsis
Cancer Genetics|April 21, 2011
Unbalanced translocations of 20q in AML and MDS often involve interstitial rather than terminal deletions of 20qRuth N MacKinnon, Hendrika M Duivenvoorden, Lynda J Campbell
Molecular Cytogenetics|December 15, 2020
Detailed molecular cytogenetic characterisation of the myeloid cell line U937 reveals the fate of homologous chromosomes and shows that centromere capture is a feature of genome instabilityRuth N MacKinnon, Joanne Peverall, Lynda J Campbell, et al.
Cancer Genetics|May 4, 2011
A cryptic deletion in 5q31.2 provides further evidence for a minimally deleted region in myelodysplastic syndromesRuth N MacKinnon, George Kannourakis, Meaghan Wall, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Methods in Molecular Biology (Clifton, N.J.)|March 23, 2018
Analysis of Chromothripsis by Combined FISH and Microarray AnalysisRuth N MacKinnon
Methods in Molecular Biology (Clifton, N.J.)|March 25, 2011
The use of M-FISH and M-BAND to define chromosome abnormalitiesRuth N Mackinnon, Ilse Chudoba
Genetics Research International|May 9, 2012
The role of dicentric chromosome formation and secondary centromere deletion in the evolution of myeloid malignancyRuth N Mackinnon, Lynda J Campbell
Cancer Genetics and Cytogenetics|December 13, 2005
A comparison of two contrasting recurrent isochromosomes 20 found in myelodysplastic syndromes suggests that retention of proximal 20q is a significant factor in myeloid malignanciesRuth N MacKinnon, Lynda J Campbell
Cancer Genetics|August 6, 2013
Chromothripsis under the microscope: a cytogenetic perspective of two cases of AML with catastrophic chromosome rearrangementRuth N Mackinnon, Lynda J Campbell
Cancer Genetics and Cytogenetics|August 17, 2005
Recurrent duplication of Xq27-qter in hematological malignancies revealed by multicolor fluorescence in situ hybridization and multicolor bandingRuth N MacKinnon, Adrian Zordan, Lynda J Campbell
Molecular Cytogenetics|March 25, 2016
Active centromere and chromosome identification in fixed cell linesThian T Beh, Ruth N MacKinnon, Paul Kalitsis
Cancer Genetics|April 21, 2011
Unbalanced translocations of 20q in AML and MDS often involve interstitial rather than terminal deletions of 20qRuth N MacKinnon, Hendrika M Duivenvoorden, Lynda J Campbell
Molecular Cytogenetics|December 15, 2020
Detailed molecular cytogenetic characterisation of the myeloid cell line U937 reveals the fate of homologous chromosomes and shows that centromere capture is a feature of genome instabilityRuth N MacKinnon, Joanne Peverall, Lynda J Campbell, et al.
Cancer Genetics|May 4, 2011
A cryptic deletion in 5q31.2 provides further evidence for a minimally deleted region in myelodysplastic syndromesRuth N MacKinnon, George Kannourakis, Meaghan Wall, et al.
Pageof 2