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Leslie R Rowe

Showing results (11-20 of 24) with videos related to

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American Journal of Clinical Pathology|March 13, 2002
The unsatisfactory ThinPrep Pap Test: missed opportunity for disease detection?Joel S Bentz, Leslie R Rowe, Evelyn V Gopez, et al.
Cancer Genetics and Cytogenetics|March 14, 2007
An inv(16) in Ph-negative cells of a chronic myelogenous leukemia patient after imatinib treatmentLeslie R Rowe, Arthur R Brothman, William E Nibley, et al.
Acta Cytologica|August 19, 2003
Accuracy of a slide profiler for endocervical cell detection in no-further-review conventional Pap smearsLeslie R Rowe, C Jay Marshall, Michael Berry, et al.
Cancer|April 21, 2004
Rapid detection of the t(11;14) translocation in mantle cell lymphoma by interphase fluorescence in situ hybridization on archival cytopathologic materialJoel S Bentz, Leslie R Rowe, Scott R Anderson, et al.
Applied Immunohistochemistry & Molecular Morphology : AIMM|June 21, 2006
Tumor cell nuclei extraction from paraffin-embedded lymphoid tissue for fluorescence in situ hybridizationLeslie R Rowe, Carlynn Willmore-Payne, Sheryl R Tripp, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|April 28, 2009
B-RAF V600E mutational analysis of fine needle aspirates correlates with diagnosis of thyroid nodulesBrandon G Bentz, Brian T Miller, Joseph A Holden, et al.
Clinical Chemistry|March 20, 2010
Enrichment and detection of rare alleles by means of snapback primers and rapid-cycle PCRLuming Zhou, Robert A Palais, G Denice Smith, et al.
American Journal of Medical Genetics. Part A|November 23, 2011
Chromosomal loss of 3q26.3-3q26.32, involving a partial neuroligin 1 deletion, identified by genomic microarray in a child with microcephaly, seizure disorder, and severe intellectual disabilityAlison Millson, Danielle Lagrave, Mary J H Willis, et al.
American Journal of Medical Genetics. Part A|August 24, 2016
Braddock-Carey syndrome: A 21q22 contiguous gene syndrome encompassing RUNX1Stephen R Braddock, Sarah T South, Joshua D Schiffman, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|June 20, 2014
Two cases of Scimitar syndrome associated with multiple congenital skeletal anomalies and lacking abnormalities by genomic microarray analysisIsaac E Lloyd, Leslie R Rowe, Lance K Erickson, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
American Journal of Clinical Pathology|March 13, 2002
The unsatisfactory ThinPrep Pap Test: missed opportunity for disease detection?Joel S Bentz, Leslie R Rowe, Evelyn V Gopez, et al.
Cancer Genetics and Cytogenetics|March 14, 2007
An inv(16) in Ph-negative cells of a chronic myelogenous leukemia patient after imatinib treatmentLeslie R Rowe, Arthur R Brothman, William E Nibley, et al.
Acta Cytologica|August 19, 2003
Accuracy of a slide profiler for endocervical cell detection in no-further-review conventional Pap smearsLeslie R Rowe, C Jay Marshall, Michael Berry, et al.
Cancer|April 21, 2004
Rapid detection of the t(11;14) translocation in mantle cell lymphoma by interphase fluorescence in situ hybridization on archival cytopathologic materialJoel S Bentz, Leslie R Rowe, Scott R Anderson, et al.
Applied Immunohistochemistry & Molecular Morphology : AIMM|June 21, 2006
Tumor cell nuclei extraction from paraffin-embedded lymphoid tissue for fluorescence in situ hybridizationLeslie R Rowe, Carlynn Willmore-Payne, Sheryl R Tripp, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|April 28, 2009
B-RAF V600E mutational analysis of fine needle aspirates correlates with diagnosis of thyroid nodulesBrandon G Bentz, Brian T Miller, Joseph A Holden, et al.
Clinical Chemistry|March 20, 2010
Enrichment and detection of rare alleles by means of snapback primers and rapid-cycle PCRLuming Zhou, Robert A Palais, G Denice Smith, et al.
American Journal of Medical Genetics. Part A|November 23, 2011
Chromosomal loss of 3q26.3-3q26.32, involving a partial neuroligin 1 deletion, identified by genomic microarray in a child with microcephaly, seizure disorder, and severe intellectual disabilityAlison Millson, Danielle Lagrave, Mary J H Willis, et al.
American Journal of Medical Genetics. Part A|August 24, 2016
Braddock-Carey syndrome: A 21q22 contiguous gene syndrome encompassing RUNX1Stephen R Braddock, Sarah T South, Joshua D Schiffman, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|June 20, 2014
Two cases of Scimitar syndrome associated with multiple congenital skeletal anomalies and lacking abnormalities by genomic microarray analysisIsaac E Lloyd, Leslie R Rowe, Lance K Erickson, et al.
Pageof 3