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Cancer Genetics and Cytogenetics
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November 1, 1996
Acute promyelocytic leukemia with t(15;16;17;19) and unusual fluorescence in situ hybridization pattern with PML and RARA probes
N R Kamal, C A Hanson, G W Dewald
Mayo Clinic Proceedings
|
July 1, 1996
Detection of hyperdiploid malignant cells in pleural effusions with chromosome-specific probes and fluorescence in situ hybridization
T M Johnson, D G Kuffel, G W Dewald
Mayo Clinic Proceedings
|
August 1, 1985
Cytogenetic studies in 174 consecutive patients with preleukemic or myelodysplastic syndromes
R H Knapp, G W Dewald, R V Pierre
Leukemia & Lymphoma
|
September 24, 1999
Atypical BCR and ABL D-FISH patterns in chronic myeloid leukemia and their possible role in therapy
G W Dewald, W A Wyatt, R T Silver
American Journal of Medical Genetics
|
May 15, 1993
Inverted duplication involving alpha satellite DNA resulting in a C-negative-band in the qh region of chromosome 16
S M Jalal, M E Law, G W Dewald
Blood
|
January 1, 1982
Three patients with structurally abnormal X chromosomes, each with Xq13 breakpoints and a history of idiopathic acquired sideroblastic anemia
G W Dewald, R V Pierre, R L Phyliky
American Journal of Clinical Pathology
|
February 1, 1986
Ph1-negative chronic granulocytic leukemia: a nonentity
L B Travis, R V Pierre, G W DeWald
Prenatal Diagnosis
|
August 1, 1992
Pseudomosaicism, true mosaicism, and maternal cell contamination in amniotic fluid processed with in situ culture and robotic harvesting
C A Moertel, P J Stupca, G W Dewald
Mayo Clinic Proceedings
|
May 1, 1997
Chronic granulocytic leukemia: recent information on pathogenesis, diagnosis, and disease monitoring
A Tefferi, M R Litzow, P Noel, et al.
Cancer Genetics and Cytogenetics
|
July 1, 1987
Trisomy 9 in hematologic disorders: possible association with primary thrombocytosis
D Cournoyer, P Noël, M A Schmidt, et al.
Page
of 13
Search research articles
Search
Showing results (11-20 of 125) with videos related to
Sort By:
Page
of 13
Cancer Genetics and Cytogenetics
|
November 1, 1996
Acute promyelocytic leukemia with t(15;16;17;19) and unusual fluorescence in situ hybridization pattern with PML and RARA probes
N R Kamal, C A Hanson, G W Dewald
Mayo Clinic Proceedings
|
July 1, 1996
Detection of hyperdiploid malignant cells in pleural effusions with chromosome-specific probes and fluorescence in situ hybridization
T M Johnson, D G Kuffel, G W Dewald
Mayo Clinic Proceedings
|
August 1, 1985
Cytogenetic studies in 174 consecutive patients with preleukemic or myelodysplastic syndromes
R H Knapp, G W Dewald, R V Pierre
Leukemia & Lymphoma
|
September 24, 1999
Atypical BCR and ABL D-FISH patterns in chronic myeloid leukemia and their possible role in therapy
G W Dewald, W A Wyatt, R T Silver
American Journal of Medical Genetics
|
May 15, 1993
Inverted duplication involving alpha satellite DNA resulting in a C-negative-band in the qh region of chromosome 16
S M Jalal, M E Law, G W Dewald
Blood
|
January 1, 1982
Three patients with structurally abnormal X chromosomes, each with Xq13 breakpoints and a history of idiopathic acquired sideroblastic anemia
G W Dewald, R V Pierre, R L Phyliky
American Journal of Clinical Pathology
|
February 1, 1986
Ph1-negative chronic granulocytic leukemia: a nonentity
L B Travis, R V Pierre, G W DeWald
Prenatal Diagnosis
|
August 1, 1992
Pseudomosaicism, true mosaicism, and maternal cell contamination in amniotic fluid processed with in situ culture and robotic harvesting
C A Moertel, P J Stupca, G W Dewald
Mayo Clinic Proceedings
|
May 1, 1997
Chronic granulocytic leukemia: recent information on pathogenesis, diagnosis, and disease monitoring
A Tefferi, M R Litzow, P Noel, et al.
Cancer Genetics and Cytogenetics
|
July 1, 1987
Trisomy 9 in hematologic disorders: possible association with primary thrombocytosis
D Cournoyer, P Noël, M A Schmidt, et al.
Page
of 13