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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 treatment
Leslie 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 smears
Leslie 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 material
Joel 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 hybridization
Leslie 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 nodules
Brandon 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 PCR
Luming 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 disability
Alison 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 RUNX1
Stephen 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 analysis
Isaac E Lloyd, Leslie R Rowe, Lance K Erickson, et al.
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of 3
Search research articles
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Showing results (11-20 of 24) with videos related to
Sort By:
Page
of 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 treatment
Leslie 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 smears
Leslie 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 material
Joel 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 hybridization
Leslie 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 nodules
Brandon 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 PCR
Luming 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 disability
Alison 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 RUNX1
Stephen 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 analysis
Isaac E Lloyd, Leslie R Rowe, Lance K Erickson, et al.
Page
of 3