Detection of the Philadelphia chromosome in interphase nuclei

E.P.J. Arnoldus, J. Wiegant, Inge Noordermeer, +5

Cytogenetic and Genome Research

Combined immunophenotyping and DNA in situ hybridization to study lineage involvement in patients with myelodysplastic syndromes

RE Kibbelaar, H van Kamp, EJ Dreef, +5

Blood

Detection of monosomy 7 and trisomy 8 in myeloid neoplasia: a comparison of banding and fluorescence in situ hybridization

RE Kibbelaar, JW Mulder, EJ Dreef, +6

Blood

Extensive cross-homology between the long and the short arm of chromosome 16 may explain leukemic inversions and translocations

JG Dauwerse, E.A. Jumelet, J. Wessels, +5

Blood

Rapid detection of chromosome 16 inversion in acute nonlymphocytic leukemia, subtype M4: regional localization of the breakpoint in 16p

Johannes G. Dauwerse, Tim Kievits, G.C. Beverstock, +7

Cytogenetic and Genome Research

CytogeneticsMixed-phenotype Acute LeukemiaGeneticsPathologyEpigenetics +18

Proliferation and cytogenetic analysis of hairy cell leukemia upon stimulation via the CD40 antigen

Hanneke C. Kluin‐Nelemans, G.C. Beverstock, P. Mollevanger, +4

Blood

Detection of 11q13 rearrangements in hematologic neoplasias by double- color fluorescence in situ hybridization

LJ Coignet, Ed Schuuring, RE Kibbelaar, +6

Blood

Translocation t(14;18) in B cell lymphomas as a cause for defective immunoglobulin production.

Daphne de Jong, B. M. H. Voetdijk, G J van Ommen, +3

The Journal of Experimental Medicine

Lymphocyte DevelopmentMixed-phenotype Acute LeukemiaImmunodeficienciesImmunologyPathology +16

De novo acute B-cell leukemia with translocation t(14;18): an entity with a poor prognosis.

M Krámer, S Raghoebier, G.C. Beverstock, +3

PubMed

Combined GTG-banding and nonradioactive in situ hybridization improves characterization of complex karyotypes

Vincent T.H.B.M. Smit, J.W. Wessels, P. Mollevanger, +4

Cytogenetic and Genome Research

CytogeneticsGeneticsMolecular BiologyGynecologyMolecular Genetics +18