Wessels HW - Search Results

1

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

van der Reijden BA, Dauwerse HG, Giles RH, Jagmohan-Changur S, Wijmenga C, Liu PP, Smit B, Wessels HW, Beverstock GC, Jotterand-Bellomo M, Martinet D, Mühlematter D, Lafage-Pochitaloff M, Gabert J, Reiffers J, Bilhou-Nabera C, van Ommen GJ, Hagemeijer A, Breuning MH. van der Reijden BA, et al. Among authors: wessels hw. Oncogene. 1999 Jan 14;18(2):543-50. doi: 10.1038/sj.onc.1202321. Oncogene. 1999. PMID: 9927211

2

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

van der Reijden BA, Lombardo M, Dauwerse HG, Giles RH, Mühlematter D, Bellomo MJ, Wessels HW, Beverstock GC, van Ommen GJ, Hagemeijer A, et al. van der Reijden BA, et al. Among authors: wessels hw. Blood. 1995 Jul 1;86(1):277-82. Blood. 1995. PMID: 7795233 Free article.

3

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

Wessels HW, Dauwerse HG, Breuning MH, Beverstock GC. Wessels HW, et al. Cancer Genet Cytogenet. 1991 Dec;57(2):225-8. doi: 10.1016/0165-4608(91)90156-o. Cancer Genet Cytogenet. 1991. PMID: 1756502 No abstract available.

4

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

Dauwerse JG, Kievits T, Beverstock GC, van der Keur D, Smit E, Wessels HW, Hagemeijer A, Pearson PL, van Ommen GJ, Breuning MH. Dauwerse JG, et al. Among authors: wessels hw. Cytogenet Cell Genet. 1990;53(2-3):126-8. doi: 10.1159/000132911. Cytogenet Cell Genet. 1990. PMID: 2369839

5

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

Beverstock GC, de Meijer PH, ten Bokkel Huinink D, Pruijt JF, den Ottolander GJ, Wessels HW, Mollevanger P. Beverstock GC, et al. Among authors: wessels hw. Cancer Genet Cytogenet. 1996 Jul 15;89(2):132-5. doi: 10.1016/0165-4608(95)00316-9. Cancer Genet Cytogenet. 1996. PMID: 8697419

6

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

Kibbelaar RE, Mulder JW, van Kamp H, Dreef EJ, Wessels HW, Beverstock GC, Haak HL, Raap AK, Kluin PM. Kibbelaar RE, et al. Among authors: wessels hw. Genes Chromosomes Cancer. 1992 Mar;4(2):128-34. doi: 10.1002/gcc.2870040205. Genes Chromosomes Cancer. 1992. PMID: 1373312

7

Trisomy 13 and myelodysplastic syndrome.

Beverstock GC, Ploem JE, Wessels H, van de Keur D, Mollevanger P. Beverstock GC, et al. Cancer Genet Cytogenet. 1990 Sep;48(2):179-82. doi: 10.1016/0165-4608(90)90117-s. Cancer Genet Cytogenet. 1990. PMID: 2397449

8

A second case of hexasomy 8 in myelodysplastic syndrome.

Beverstock GC, Wessels HW, Mollevanger P, den Ottolander GJ, Gottlieb DJ. Beverstock GC, et al. Among authors: wessels hw. Cancer Genet Cytogenet. 1997 Nov;99(1):68-72. doi: 10.1016/s0165-4608(96)00441-4. Cancer Genet Cytogenet. 1997. PMID: 9352798 Review.

9

Identification of RUNX1/AML1 as a classical tumor suppressor gene.

Silva FP, Morolli B, Storlazzi CT, Anelli L, Wessels H, Bezrookove V, Kluin-Nelemans HC, Giphart-Gassler M. Silva FP, et al. Oncogene. 2003 Jan 30;22(4):538-47. doi: 10.1038/sj.onc.1206141. Oncogene. 2003. PMID: 12555067

10

Chromosome abnormalities in a patient with acquired immunodeficiency syndrome (AIDS) and Burkitt lymphoma-leukemia.

Beverstock GC, Roozendaal KJ, Bödvarsson A, Jonkers GJ, van de Keur D, Wessels H, Webster MR. Beverstock GC, et al. Leukemia. 1990 Jun;4(6):445-7. Leukemia. 1990. PMID: 2163000 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

22 results

Search Page

Filters