Beverstock GC - Search Results

1

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

Dauwerse JG, Jumelet EA, Wessels JW, Saris JJ, Hagemeijer A, Beverstock GC, van Ommen GJ, Breuning MH. Dauwerse JG, et al. Among authors: beverstock gc. Blood. 1992 Mar 1;79(5):1299-304. Blood. 1992. PMID: 1536953 Free article.

2

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. Among authors: beverstock gc. 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.

3

Improved interpretation of complex chromosomal rearrangements by combined GTG banding and in situ suppression hybridization using chromosome-specific libraries and cosmid probes.

Smit VT, Wessels JW, Mollevanger P, Dauwerse JG, van Vliet M, Beverstock GC, Breuning MH, Devilee P, Raap AK, Cornelisse CJ. Smit VT, et al. Among authors: beverstock gc. Genes Chromosomes Cancer. 1991 Jul;3(4):239-48. doi: 10.1002/gcc.2870030402. Genes Chromosomes Cancer. 1991. PMID: 1958589

4

Two distinct loci on the short arm of chromosome 16 are involved in myeloid leukemia.

Wessels JW, Mollevanger P, Dauwerse JG, Cluitmans FH, Breuning MH, Beverstock GC. Wessels JW, et al. Among authors: beverstock gc. Blood. 1991 Apr 1;77(7):1555-9. Blood. 1991. PMID: 2009371 Free article.

5

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: beverstock gc. Cytogenet Cell Genet. 1990;53(2-3):126-8. doi: 10.1159/000132911. Cytogenet Cell Genet. 1990. PMID: 2369839

6

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: beverstock gc. Blood. 1995 Jul 1;86(1):277-82. Blood. 1995. PMID: 7795233 Free article.

7

A gene for a myosin peptide is disrupted by the inv(16)(p13q22) in acute nonlymphocytic leukemia M4Eo.

van der Reijden BA, Dauwerse JG, Wessels JW, Beverstock GC, Hagemeijer A, van Ommen GJ, Breuning MH. van der Reijden BA, et al. Among authors: beverstock gc. Blood. 1993 Nov 15;82(10):2948-52. Blood. 1993. PMID: 8219185 Free article.

8

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

Kibbelaar RE, Mulder JW, Dreef EJ, van Kamp H, Fibbe WE, Wessels JW, Beverstock GC, Haak HL, Kluin PM. Kibbelaar RE, et al. Among authors: beverstock gc. Blood. 1993 Aug 1;82(3):904-13. Blood. 1993. PMID: 8338953 Free article.

9

Rubinstein-Taybi syndrome caused by submicroscopic deletions within 16p13.3.

Breuning MH, Dauwerse HG, Fugazza G, Saris JJ, Spruit L, Wijnen H, Tommerup N, van der Hagen CB, Imaizumi K, Kuroki Y, van den Boogaard MJ, de Pater JM, Mariman EC, Hamel BC, Himmelbauer H, Frischauf AM, Stallings R, Beverstock GC, van Ommen GJ, Hennekam RC. Breuning MH, et al. Among authors: beverstock gc. Am J Hum Genet. 1993 Feb;52(2):249-54. Am J Hum Genet. 1993. PMID: 8430691 Free PMC article.

10

Simple method for detection of MYH11 DNA rearrangements in patients with inv(16)(p13q22) and acute myeloid leukemia.

van der Reijden BA, Martinet D, Dauwerse JG, Giles RH, Wessels JW, Beverstock GC, Smit B, Mühlematter D, Jotterand Bellomo M, Gabert J, Lafage-Pochitaloff M, Reiffers J, Bilhou-Nabera C, van Ommen GJ, Hagemeijer A, Breuning MH. van der Reijden BA, et al. Among authors: beverstock gc. Leukemia. 1996 Sep;10(9):1459-62. Leukemia. 1996. PMID: 8751463

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