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Cancer Genetics and Cytogenetics|December 8, 2009
Identification of chromosomal abnormalities relevant to prognosis in chronic lymphocytic leukemia using multiplex ligation-dependent probe amplificationMarian Stevens-Kroef, Annet Simons, Hanneke Gorissen, et al.
Genes, Chromosomes & Cancer|July 27, 2012
High detection rate of clinically relevant genomic abnormalities in plasma cells enriched from patients with multiple myelomaMarian Stevens-Kroef, Daniel Olde Weghuis, Sandra Croockewit, et al.
European Journal of Medical Genetics|August 12, 2008
Detection of cryptic subtelomeric imbalances in fetuses with ultrasound abnormalitiesBrigitte H W Faas, Willy Nillesen, Sascha Vermeer, et al.
Molecular Cytogenetics|January 10, 2014
Identification of prognostic relevant chromosomal abnormalities in chronic lymphocytic leukemia using microarray-based genomic profilingMarian Jpl Stevens-Kroef, Eva van den Berg, Daniel Olde Weghuis, et al.
Genes, Chromosomes & Cancer|September 2, 2011
Microarray-based genomic profiling as a diagnostic tool in acute lymphoblastic leukemiaAnnet Simons, Marian Stevens-Kroef, Najat El Idrissi-Zaynoun, et al.
American Journal of Medical Genetics. Part A|April 14, 2007
Dandy-Walker complex in a boy with a 5 Mb deletion of region 1q44 due to a paternal t(1;20)(q44;q13.33)Martin Poot, Hester Y Kroes, Suzanne E V D Wijst, et al.
American Journal of Human Genetics|July 8, 2021
Next-generation cytogenetics: Comprehensive assessment of 52 hematological malignancy genomes by optical genome mappingKornelia Neveling, Tuomo Mantere, Susan Vermeulen, et al.
American Journal of Hematology|January 2, 2024
A framework for the clinical implementation of optical genome mapping in hematologic malignanciesBrynn Levy, Rashmi Kanagal-Shamanna, Nikhil S Sahajpal, et al.
American Journal of Human Genetics|July 8, 2021
Optical genome mapping enables constitutional chromosomal aberration detectionTuomo Mantere, Kornelia Neveling, Céline Pebrel-Richard, et al.
Genes, Chromosomes & Cancer|February 26, 2017
Genomic array as compared to karyotyping in myelodysplastic syndromes in a prospective clinical trialMarian J Stevens-Kroef, Daniel Olde Weghuis, Najat ElIdrissi-Zaynoun, et al.
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