H. Wessels

发表

Identification of RUNX1/AML1 as a classical tumor suppressor gene

M. Giphart-Gassler, H. Kluin-Nelemans, B. Morolli, 2003, Oncogene.

Inversion 16 and translocation (16;16) in ANLL M4eo break in the same subregion of the short arm of chromosome 16.

G. Beverstock, H. Wessels, H. Dauwerse, 1991, Cancer genetics and cytogenetics.

Genome wide molecular analysis of minimally differentiated acute myeloid leukemia

R. Vossen, M. Giphart-Gassler, H. Kluin-Nelemans, 2009, Haematologica.

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

A. Hagemeijer, P. Pearson, M. Breuning, 1990, Cytogenetics and cell genetics.

Genomic amplification of MYC as double minutes in a patient with APL-like leukemia

G. Ossenkoppele, H. Wessels, S. Zweegman, 2014, Molecular Cytogenetics.

RT-PCR diagnosis of patients with acute nonlymphocytic leukemia and inv(16)(p13q22) and identification of new alternative splicing in CBFB-MYH11 transcripts.

A. Hagemeijer, B. V. D. Reijden, R. Giles, 1995, Blood.

Paragangliomas of the head and neck region show complete loss of heterozygosity at 11q22-q23 in chief cells and the flow-sorted DNA aneuploid fraction.

P. Devilee, M. Beekman, C. Cornelisse, 1998, Human pathology.

Trisomy 13 and myelodysplastic syndrome.

G. Beverstock, H. Wessels, P. Mollevanger, 1990, Cancer genetics and cytogenetics.

The heterogeneous distribution of monosomy 3 in uveal melanomas: implications for prognostication based on fine-needle aspiration biopsies.

E. Jordanova, N. Schalij-Delfos, M. Jager, 2007, Archives of pathology & laboratory medicine.

A novel chromosomal translocation t(3;5)(q12;p15.3) and loss of heterozygosity on chromosome 22 in a multifocal follicular variant of papillary thyroid carcinoma presenting with skin metastases

H. Morreau, S. V. van Zelderen-Bhola, H. Wessels, 2001, Clinical endocrinology.

Translocations (X;10)(p22;q24) and (1;10)(q21;q11) in a follicular adenoma of the thyroid without apparent involvement of the RET protooncogene.

R. Vink, J. Smit, S. V. van Zelderen-Bhola, 1999, Cancer genetics and cytogenetics.

Ring chromosome 4 as the sole cytogenetic anomaly in a chondroblastoma: a case report and review of the literature.

P. Hogendoorn, A. Taminiau, J. Bovée, 1998, Cancer genetics and cytogenetics.

A second case of hexasomy 8 in myelodysplastic syndrome.

G. Beverstock, G. Den Ottolander, H. Wessels, 1997, Cancer genetics and cytogenetics.

Effect of mast cell growth factor (c-kit ligand) on clonogenic leukemic precursor cells.

D. Williams, J. Falkenburg, R. Willemze, 1992, Blood.

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

J. Falkenburg, R. Willemze, H. Kluin-Nelemans, 1994, Blood.

Nonradioactive in situ hybridisation of the translocation t(1;7) in myeloid malignancies

A. Raap, P. Kluin, G. Beverstock, 1992, Genes, chromosomes & cancer.

Genomic amplification of MYC as double minutes in a patient with APL-like leukemia

G. Ossenkoppele, H. Wessels, S. Zweegman, 2014, Molecular Cytogenetics.

Sublocalization of the breakpoints of a t(5;16) in myelodysplasia.

A. V. van Kessel, R. Willemze, B. Janssen, 1998, Cancer genetics and cytogenetics.

Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clustered

C. Wijmenga, A. Hagemeijer, J. Gabert, 1999, Oncogene.

Characterization of a New Human B Cell Line (Bonna-12) with Trisomy 9 and Trisomy 12 Chromosomal Abnormality.

H. Kluin-Nelemans, J. Jansen, G. Beverstock, 1991, Leukemia & lymphoma.

A case of isodicentric 7p as sole abnormality in a patient with acute myeloid leukemia.

J. Pruijt, D. ten Bokkel Huinink, G. Beverstock, 1996, Cancer genetics and cytogenetics.