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A R Brothman

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Cancer Genetics and Cytogenetics|November 11, 1998
Chromosome 7 abnormalities in prostate cancer detected by dual-color fluorescence in situ hybridizationJ Cui, D A Deubler, L R Rohr, et al.
Archives of Pathology & Laboratory Medicine|April 1, 1997
Pilot studies for proficiency testing using fluorescence in situ hybridization with chromosome-specific DNA probes: a College of American Pathologists/American College of Medical Genetics ProgramG W Dewald, A R Brothman, M G Butler, et al.
Genes, Chromosomes & Cancer|July 21, 1998
Commonly occurring loss and mutation of the MXI1 gene in prostate cancerE V Prochownik, L Eagle Grove, D Deubler, et al.
Cancer Genetics and Cytogenetics|August 1, 1991
Cytogenetic evaluation of 20 cultured primary prostatic tumorsA R Brothman, D M Peehl, A M Patel, et al.
Genomics|February 15, 2001
A common deletion at chromosomal region 17q21 in sporadic prostate tumors distal to BRCA1Q Dai, D A Deubler, T M Maxwell, et al.
Journal of Medical Genetics|January 8, 2008
Comparison of targeted and whole genome analysis of postnatal specimens using a commercially available array based comparative genomic hybridisation (aCGH) microarray platformE Aston, H Whitby, T Maxwell, et al.
Cancer Genetics and Cytogenetics|December 5, 2000
Microdissection, DOP-PCR, and comparative genomic hybridization of paraffin-embedded familial prostate cancersP C Verhagen, X L Zhu, L R Rohr, et al.
Journal of Medical Genetics|April 17, 2008
Expansion in size of a terminal deletion: a paradigm shift for parental follow-up studiesS T South, A F Rope, A N Lamb, et al.
Cancer Genetics and Cytogenetics|December 6, 2001
Cytogenetic-clinicopathologic correlations in rhabdomyosarcoma: a report of five casesZ Chen, C M Coffin, L M Smith, et al.
Cytogenetic and Genome Research|March 17, 2009
Benign copy number changes in clinical cytogenetic diagnostics by array CGHH Whitby, A Tsalenko, E Aston, et al.
Pageof 8

Showing results (61-70 of 78) with videos related to

Sort By:
Pageof 8
Cancer Genetics and Cytogenetics|November 11, 1998
Chromosome 7 abnormalities in prostate cancer detected by dual-color fluorescence in situ hybridizationJ Cui, D A Deubler, L R Rohr, et al.
Archives of Pathology & Laboratory Medicine|April 1, 1997
Pilot studies for proficiency testing using fluorescence in situ hybridization with chromosome-specific DNA probes: a College of American Pathologists/American College of Medical Genetics ProgramG W Dewald, A R Brothman, M G Butler, et al.
Genes, Chromosomes & Cancer|July 21, 1998
Commonly occurring loss and mutation of the MXI1 gene in prostate cancerE V Prochownik, L Eagle Grove, D Deubler, et al.
Cancer Genetics and Cytogenetics|August 1, 1991
Cytogenetic evaluation of 20 cultured primary prostatic tumorsA R Brothman, D M Peehl, A M Patel, et al.
Genomics|February 15, 2001
A common deletion at chromosomal region 17q21 in sporadic prostate tumors distal to BRCA1Q Dai, D A Deubler, T M Maxwell, et al.
Journal of Medical Genetics|January 8, 2008
Comparison of targeted and whole genome analysis of postnatal specimens using a commercially available array based comparative genomic hybridisation (aCGH) microarray platformE Aston, H Whitby, T Maxwell, et al.
Cancer Genetics and Cytogenetics|December 5, 2000
Microdissection, DOP-PCR, and comparative genomic hybridization of paraffin-embedded familial prostate cancersP C Verhagen, X L Zhu, L R Rohr, et al.
Journal of Medical Genetics|April 17, 2008
Expansion in size of a terminal deletion: a paradigm shift for parental follow-up studiesS T South, A F Rope, A N Lamb, et al.
Cancer Genetics and Cytogenetics|December 6, 2001
Cytogenetic-clinicopathologic correlations in rhabdomyosarcoma: a report of five casesZ Chen, C M Coffin, L M Smith, et al.
Cytogenetic and Genome Research|March 17, 2009
Benign copy number changes in clinical cytogenetic diagnostics by array CGHH Whitby, A Tsalenko, E Aston, et al.
Pageof 8