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The Utilization of Chromosomal Microarray Technologies for Hematologic Neoplasms: An ACLPS Critical Review.
- Published in:
- 2018
- By:
- Publication type:
- journal article
A Test Utilization Approach to the Diagnostic Workup of Isolated Eosinophilia in Otherwise Morphologically Unremarkable Bone Marrow: A Single Institutional Experience.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Phenotypic characterization, karyotype analysis and in vitro tamoxifen sensitivity of new ER-negative vulvar carcinoma cell lines, UM-SCV-1A and UM-SCV-1B.
- Published in:
- International Journal of Cancer, 1990, v. 45, n. 5, p. 920, doi. 10.1002/ijc.2910450524
- By:
- Publication type:
- Article
Advanced Maternal Age in Polyploidy With Concurrent Aneuploidy.
- Published in:
- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 5, p. 1200, doi. 10.1002/ajmg.a.35870
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- Publication type:
- Article
Two regions of homozygosity on chromosome 3p in squamous cell carcinoma of the head and neck: Comparison with cytogenetic analysis.
- Published in:
- Head & Neck, 1996, v. 18, n. 6, p. 529, doi. 10.1002/(SICI)1097-0347(199611/12)18:6<529::AID-HED7>3.0.CO;2-4
- By:
- Publication type:
- Article
The Dohner fluorescence in situ hybridization prognostic classification of chronic lymphocytic leukaemia ( CLL): the CLL Research Consortium experience.
- Published in:
- British Journal of Haematology, 2016, v. 173, n. 1, p. 105, doi. 10.1111/bjh.13933
- By:
- Publication type:
- Article
Identification of recurrent truncated DDX3X mutations in chronic lymphocytic leukaemia.
- Published in:
- British Journal of Haematology, 2015, v. 169, n. 3, p. 445, doi. 10.1111/bjh.13211
- By:
- Publication type:
- Article
Patients with chronic lymphocytic leukaemia and clonal deletion of both 17p13.1 and 11q22.3 have a very poor prognosis.
- Published in:
- British Journal of Haematology, 2013, v. 163, n. 3, p. 326, doi. 10.1111/bjh.12534
- By:
- Publication type:
- Article
Allelic Loss and Tumor Pathology in Head and Neck Squamous Cell Carcinoma.
- Published in:
- Modern Pathology, 2003, v. 16, n. 10, p. 970, doi. 10.1097/01.MP.0000086627.74271.13
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- Publication type:
- Article
Typical, atypical and cryptic t(15;17)(q24;q21) (PML::RARA) observed in acute promyelocytic leukemia: A retrospective review of 831 patients with concurrent chromosome and PML::RARA dual‐color dual‐fusion FISH studies.
- Published in:
- Genes, Chromosomes & Cancer, 2022, v. 61, n. 10, p. 629, doi. 10.1002/gcc.23070
- By:
- Publication type:
- Article
Isochromosome 5p mosaicism at prenatal diagnosis: observations and outcomes in six cases at chorionic villus sampling and one at amniocentesis.
- Published in:
- Prenatal Diagnosis, 2002, v. 22, n. 8, p. 681, doi. 10.1002/pd.379
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- Publication type:
- Article
Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlations.
- Published in:
- 1997
- By:
- Publication type:
- journal article
INCIDENCE AND SIGNIFICANCE OF CHROMOSOME MOSAICISM INVOLVING AN AUTOSOMAL STRUCTURAL ABNORMALITY DIAGNOSED PRENATALLY THROUGH AMNIOCENTESIS: A COLLABORATIVE STUDY.
- Published in:
- Prenatal Diagnosis, 1996, v. 16, n. 1, p. 1, doi. 10.1002/(SICI)1097-0223(199601)16:1<1::AID-PD816>3.0.CO;2-W
- By:
- Publication type:
- Article
Mosaicism for trisomy 12: four cases with varying outcomes.
- Published in:
- 1995
- By:
- Publication type:
- journal article
Trisomy 20 mosaicism identified prenatally and confirmed in foreskin fibroblasts.
- Published in:
- Prenatal Diagnosis, 1989, v. 9, n. 8, p. 601, doi. 10.1002/pd.1970090810
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- Publication type:
- Article
Chromosome 1 deletion associated with increased nuchal fold thickness in the second trimester.
- Published in:
- Prenatal Diagnosis, 1989, v. 9, n. 2, p. 141, doi. 10.1002/pd.1970090212
- By:
- Publication type:
- Article
The prognostic significance of del6q23 in chronic lymphocytic leukemia.
- Published in:
- American Journal of Hematology, 2021, v. 96, n. 6, p. E203, doi. 10.1002/ajh.26168
- By:
- Publication type:
- Article
Chromosomal biomarkers in the clonal evolution of head and neck squamous neoplasia.
- Published in:
- Journal of Cellular Biochemistry, 1993, v. 53, p. 213, doi. 10.1002/jcb.240531032
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- Publication type:
- Article
Deletion 9p22-pter and loss of Y as primary chromosome abnormalities in a squamous cell carcinoma of the vocal cord.
- Published in:
- Genes, Chromosomes & Cancer, 1993, v. 6, n. 1, p. 58, doi. 10.1002/gcc.2870060111
- By:
- Publication type:
- Article
Consistent Chromosome Abnormalities in Squamous Cell Carcinoma of the Vulva.
- Published in:
- Genes, Chromosomes & Cancer, 1991, v. 3, n. 6, p. 420, doi. 10.1002/gcc.2870030604
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- Publication type:
- Article
11p Deletions and breakpoints in squamous cell carcinoma: Association with altered reactivity with the UM-E7 antibody.
- Published in:
- Genes, Chromosomes & Cancer, 1991, v. 3, n. 4, p. 272, doi. 10.1002/gcc.2870030406
- By:
- Publication type:
- Article
Utility of Targeted Sequencing Compared to FISH for Detection of Chronic Lymphocytic Leukemia Copy Number Alterations.
- Published in:
- Cancers, 2024, v. 16, n. 13, p. 2450, doi. 10.3390/cancers16132450
- By:
- Publication type:
- Article
MCIR1: A patient‐derived mantle cell lymphoma line for discovering new treatments for ibrutinib resistance.
- Published in:
- European Journal of Haematology, 2021, v. 107, n. 4, p. 458, doi. 10.1111/ejh.13682
- By:
- Publication type:
- Article
The Utilization of Chromosomal Microarray Technologies for Hematologic NeoplasmsAn ACLPS Critical Review.
- Published in:
- American Journal of Clinical Pathology, 2018, v. 150, n. 5, p. 375, doi. 10.1093/ajcp/aqy076
- By:
- Publication type:
- Article
A Test Utilization Approach to the Diagnostic Workup of Isolated Eosinophilia in Otherwise Morphologically Unremarkable Bone MarrowA Single Institutional Experience.
- Published in:
- American Journal of Clinical Pathology, 2018, v. 150, n. 5, p. 421, doi. 10.1093/ajcp/aqy064
- By:
- Publication type:
- Article
Bone Marrow Conventional Karyotyping and Fluorescence In Situ Hybridization: Defining an Effective Utilization Strategy for Evaluation of Myelodysplastic Syndromes.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Bone Marrow Conventional Karyotyping and Fluorescence In Situ Hybridization.
- Published in:
- American Journal of Clinical Pathology, 2016, v. 146, n. 1, p. 86, doi. 10.1093/AJCP/AQW077
- By:
- Publication type:
- Article
Is It Time for a New Gold Standard? FISH vs Cytogenetics in AML Diagnosis.
- Published in:
- 2016
- By:
- Publication type:
- Letter
The Authors' Reply.
- Published in:
- 2016
- By:
- Publication type:
- Letter to the Editor
Conventional karyotyping and fluorescence in situ hybridization: an effective utilization strategy in diagnostic adult acute myeloid leukemia.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Conventional Karyotyping and Fluorescence In Situ Hybridization.
- Published in:
- American Journal of Clinical Pathology, 2015, v. 143, n. 6, p. 873, doi. 10.1309/AJCPP6LVMQG4LNCK
- By:
- Publication type:
- Article
Cover Image.
- Published in:
- 2019
- By:
- Publication type:
- Cover Art
Mate pair sequencing improves detection of genomic abnormalities in acute myeloid leukemia.
- Published in:
- European Journal of Haematology, 2019, v. 102, n. 1, p. 87, doi. 10.1111/ejh.13179
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- Publication type:
- Article
Conventional cytogenetics in myelofibrosis: literature review and discussion.
- Published in:
- European Journal of Haematology, 2009, v. 82, n. 5, p. 329, doi. 10.1111/j.1600-0609.2009.01224.x
- By:
- Publication type:
- Article
Karyotype complements the International Prognostic Scoring System for primary myelofibrosis.
- Published in:
- European Journal of Haematology, 2009, v. 82, n. 4, p. 255, doi. 10.1111/j.1600-0609.2009.01216.x
- By:
- Publication type:
- Article
Peripheral blood cytogenetic studies in hematological neoplasms: predictors of obtaining metaphases for analysis.
- Published in:
- European Journal of Haematology, 2008, v. 80, n. 4, p. 318, doi. 10.1111/j.1600-0609.2007.01021.x
- By:
- Publication type:
- Article
Significance of p53 mutations in patients with chronic lymphocytic leukemia: a sequential study of 30 patients.
- Published in:
- 2001
- By:
- Publication type:
- journal article
Defining clear cell papillary renal cell carcinoma in routine clinical practice.
- Published in:
- Histopathology, 2020, v. 76, n. 7, p. 1093, doi. 10.1111/his.14071
- By:
- Publication type:
- Article
Prognostic implications of loss of heterozygosity at 8p21 and 9p21 in head and neck squamous cell carcinoma.
- Published in:
- International Journal of Cancer, 2004, v. 111, n. 2, p. 206, doi. 10.1002/ijc.20254
- By:
- Publication type:
- Article
A rapid and reliable chromosome analysis method for products of conception using interphase nuclei.
- Published in:
- Molecular Genetics & Genomic Medicine, 2018, v. 6, n. 3, p. 370, doi. 10.1002/mgg3.381
- By:
- Publication type:
- Article
Clinical outcomes in patients with chronic lymphocytic leukemia with disease progression on ibrutinib.
- Published in:
- Blood Cancer Journal, 2022, v. 12, n. 9, p. 1, doi. 10.1038/s41408-022-00721-6
- By:
- Publication type:
- Article
Distinct immune signatures in chronic lymphocytic leukemia and Richter syndrome.
- Published in:
- Blood Cancer Journal, 2021, v. 11, n. 5, p. 1, doi. 10.1038/s41408-021-00477-5
- By:
- Publication type:
- Article
Venetoclax treatment of patients with relapsed T-cell prolymphocytic leukemia.
- Published in:
- 2021
- By:
- Publication type:
- Letter
Evaluating current policy for detecting mosaicism in amniotic fluid cultures: implications for current cell counting practices.
- Published in:
- Statistics in Medicine, 2005, v. 24, n. 4, p. 615, doi. 10.1002/sim.2040
- By:
- Publication type:
- Article
PRDX4, a member of the peroxiredoxin family, is fused to AML1 (RUNX1) in an acute myeloid leukemia patient with a t(X;21)(p22;q22).
- Published in:
- Genes, Chromosomes & Cancer, 2004, v. 40, n. 4, p. 365, doi. 10.1002/gcc.20050
- By:
- Publication type:
- Article
Clinical significance of Y chromosome loss in hematologic disease.
- Published in:
- Genes, Chromosomes & Cancer, 2000, v. 27, n. 1, p. 11, doi. 10.1002/(SICI)1098-2264(200001)27:1<11::AID-GCC2>3.0.CO;2-I
- By:
- Publication type:
- Article
Loss of 18q predicts poor survival of patients with squamous cell carcinoma of the head and neck.
- Published in:
- Genes, Chromosomes & Cancer, 1998, v. 21, n. 4, p. 333, doi. 10.1002/(SICI)1098-2264(199804)21:4<333::AID-GCC7>3.0.CO;2-#
- By:
- Publication type:
- Article
Recurrent cytogenetic abnormalities in squamous cell carcinomas of the head and neck region.
- Published in:
- Genes, Chromosomes & Cancer, 1994, v. 9, n. 3, p. 192, doi. 10.1002/gcc.2870090308
- By:
- Publication type:
- Article
Clonal cytogenetic evolution in a squamous cell carcinoma of the skin from a xeroderma pigmentosum patient.
- Published in:
- Genes, Chromosomes & Cancer, 1993, v. 7, n. 3, p. 158, doi. 10.1002/gcc.2870070308
- By:
- Publication type:
- Article
Differential transcriptomic profiling in ibrutinib‐naïve versus ibrutinib‐resistant Richter syndrome.
- Published in:
- Hematological Oncology, 2022, v. 40, n. 2, p. 302, doi. 10.1002/hon.2950
- By:
- Publication type:
- Article