Search research articles
Contact Us
Filters
Showing results (11-20 of 85) with videos related to
Page
of 9
Sort By:
Cancer Genetics and Cytogenetics
|
October 24, 2002
Correlation of three methods of measuring cytogenetic response in chronic myelocytic leukemia
Martin L Lesser, Gordon W Dewald, Cristina P Sison, et al.
Mayo Clinic Proceedings
|
January 8, 2004
Primer on medical genomics. Part XI: Visualizing human chromosomes
Jack L Spurbeck, Sara Anne Adams, Peggy J Stupca, et al.
Cancer Genetics and Cytogenetics
|
August 26, 2003
New highly sensitive fluorescence in situ hybridization method to detect PML/RARA fusion in acute promyelocytic leukemia
Stephanie R Brockman, Sarah F Paternoster, Rhett P Ketterling, et al.
Leukemia & Lymphoma
|
May 11, 2002
The prognostic significance of trisomy 8 in patients with acute myeloid leukemia
Michelle A Elliott, Louis Letendre, Curtis A Hanson, et al.
European Journal of Haematology
|
January 19, 2005
Clinical correlates of submicroscopic deletions involving the ABL-BCR translocation region in chronic myeloid leukemia
Yinlee Yoong, Todd J VanDeWalker, Richard O Carlson, et al.
Leukemia Research
|
January 23, 2003
Clonal cytogenetic abnormalities in bone marrow specimens without clear morphologic evidence of dysplasia: a form fruste of myelodysplasia?
David P Steensma, Gordon W Dewald, Janice M Hodnefield, et al.
Leukemia & Lymphoma
|
October 11, 2007
Philadelphia chromosome mosaicism at diagnosis in chronic myeloid leukemia: clinical correlates and effect on imatinib mesylate treatment outcome
Andrew P Landstrom, Ryan A Knudson, Gordon W Dewald, et al.
Mayo Clinic Proceedings
|
August 14, 2002
Primer on medical genomics part I: History of genetics and sequencing of the human genome
Cindy Pham Lorentz, Eric D Wieben, Ayale Tefferi, et al.
Cancer Genetics and Cytogenetics
|
December 31, 2003
A novel tricolor, dual-fusion fluorescence in situ hybridization method to detect BCR/ABL fusion in cells with t(9;22)(q34;q11.2) associated with deletion of DNA on the derivative chromosome 9 in chronic myelocytic leukemia
Stephanie A Smoley, Stephanie R Brockman, Sarah F Paternoster, et al.
Cancer
|
March 29, 2006
Presence of unfavorable cytogenetic abnormalities is the strongest predictor of poor survival in secondary myelofibrosis
David Dingli, Susan M Schwager, Ruben A Mesa, et al.
Page
of 9
Search research articles
Search
Showing results (11-20 of 85) with videos related to
Sort By:
Page
of 9
Cancer Genetics and Cytogenetics
|
October 24, 2002
Correlation of three methods of measuring cytogenetic response in chronic myelocytic leukemia
Martin L Lesser, Gordon W Dewald, Cristina P Sison, et al.
Mayo Clinic Proceedings
|
January 8, 2004
Primer on medical genomics. Part XI: Visualizing human chromosomes
Jack L Spurbeck, Sara Anne Adams, Peggy J Stupca, et al.
Cancer Genetics and Cytogenetics
|
August 26, 2003
New highly sensitive fluorescence in situ hybridization method to detect PML/RARA fusion in acute promyelocytic leukemia
Stephanie R Brockman, Sarah F Paternoster, Rhett P Ketterling, et al.
Leukemia & Lymphoma
|
May 11, 2002
The prognostic significance of trisomy 8 in patients with acute myeloid leukemia
Michelle A Elliott, Louis Letendre, Curtis A Hanson, et al.
European Journal of Haematology
|
January 19, 2005
Clinical correlates of submicroscopic deletions involving the ABL-BCR translocation region in chronic myeloid leukemia
Yinlee Yoong, Todd J VanDeWalker, Richard O Carlson, et al.
Leukemia Research
|
January 23, 2003
Clonal cytogenetic abnormalities in bone marrow specimens without clear morphologic evidence of dysplasia: a form fruste of myelodysplasia?
David P Steensma, Gordon W Dewald, Janice M Hodnefield, et al.
Leukemia & Lymphoma
|
October 11, 2007
Philadelphia chromosome mosaicism at diagnosis in chronic myeloid leukemia: clinical correlates and effect on imatinib mesylate treatment outcome
Andrew P Landstrom, Ryan A Knudson, Gordon W Dewald, et al.
Mayo Clinic Proceedings
|
August 14, 2002
Primer on medical genomics part I: History of genetics and sequencing of the human genome
Cindy Pham Lorentz, Eric D Wieben, Ayale Tefferi, et al.
Cancer Genetics and Cytogenetics
|
December 31, 2003
A novel tricolor, dual-fusion fluorescence in situ hybridization method to detect BCR/ABL fusion in cells with t(9;22)(q34;q11.2) associated with deletion of DNA on the derivative chromosome 9 in chronic myelocytic leukemia
Stephanie A Smoley, Stephanie R Brockman, Sarah F Paternoster, et al.
Cancer
|
March 29, 2006
Presence of unfavorable cytogenetic abnormalities is the strongest predictor of poor survival in secondary myelofibrosis
David Dingli, Susan M Schwager, Ruben A Mesa, et al.
Page
of 9