Debiec-Rychter M - Search Results

1

Cutaneous aneurysmal fibrous histiocytoma with a t(12;19)(p12;q13) as the sole cytogenetic anomaly.

Botrus G, Sciot R, Debiec-Rychter M. Botrus G, et al. Cancer Genet Cytogenet. 2006 Jan 15;164(2):155-8. doi: 10.1016/j.cancergencyto.2005.08.020. Cancer Genet Cytogenet. 2006. PMID: 16434321

2

Spindle-cell rhabdomyosarcoma with 2q36 approximately q37 involvement.

Debiec-Rychter M, Hagemeijer A, Sciot R. Debiec-Rychter M, et al. Cancer Genet Cytogenet. 2003 Jan 1;140(1):62-5. doi: 10.1016/s0165-4608(02)00647-7. Cancer Genet Cytogenet. 2003. PMID: 12550761

3

Common chromosome aberrations in the proximal type of epithelioid sarcoma.

Debiec-Rychter M, Sciot R, Hagemeijer A. Debiec-Rychter M, et al. Cancer Genet Cytogenet. 2000 Dec;123(2):133-6. doi: 10.1016/s0165-4608(00)00320-4. Cancer Genet Cytogenet. 2000. PMID: 11150604 Review.

4

Is 4q13 a recurring breakpoint in solitary fibrous tumors?

Debiec-Rychter M, de Wever I, Hagemeijer A, Sciot R. Debiec-Rychter M, et al. Cancer Genet Cytogenet. 2001 Nov;131(1):69-73. doi: 10.1016/s0165-4608(01)00489-7. Cancer Genet Cytogenet. 2001. PMID: 11734322

5

Rectal gastrointestinal stromal tumors associated with a novel germline KIT mutation.

Woźniak A, Rutkowski P, Sciot R, Ruka W, Michej W, Debiec-Rychter M. Woźniak A, et al. Int J Cancer. 2008 May 1;122(9):2160-4. doi: 10.1002/ijc.23338. Int J Cancer. 2008. PMID: 18183595

6

Pathogenesis of vestibular schwannoma in ring chromosome 22.

Denayer E, Brems H, de Cock P, Evans GD, Van Calenbergh F, Bowers N, Sciot R, Debiec-Rychter M, Vermeesch JV, Fryns JP, Legius E. Denayer E, et al. BMC Med Genet. 2009 Sep 22;10:97. doi: 10.1186/1471-2350-10-97. BMC Med Genet. 2009. PMID: 19772601 Free PMC article.

7

The t(X;6) in subungual exostosis results in transcriptional deregulation of the gene for insulin receptor substrate 4.

Mertens F, Möller E, Mandahl N, Picci P, Perez-Atayde AR, Samson I, Sciot R, Debiec-Rychter M. Mertens F, et al. Int J Cancer. 2011 Jan 15;128(2):487-91. doi: 10.1002/ijc.25353. Int J Cancer. 2011. PMID: 20340132

8

Biallelic inactivation of NF1 in a sporadic plexiform neurofibroma.

Beert E, Brems H, Renard M, Ferreiro JF, Melotte C, Thoelen R, De Wever I, Sciot R, Legius E, Debiec-Rychter M. Beert E, et al. Genes Chromosomes Cancer. 2012 Sep;51(9):852-7. doi: 10.1002/gcc.21969. Epub 2012 May 14. Genes Chromosomes Cancer. 2012. PMID: 22585738

9

Identification of a novel, recurrent MBTD1-CXorf67 fusion in low-grade endometrial stromal sarcoma.

Dewaele B, Przybyl J, Quattrone A, Finalet Ferreiro J, Vanspauwen V, Geerdens E, Gianfelici V, Kalender Z, Wozniak A, Moerman P, Sciot R, Croce S, Amant F, Vandenberghe P, Cools J, Debiec-Rychter M. Dewaele B, et al. Int J Cancer. 2014 Mar 1;134(5):1112-22. doi: 10.1002/ijc.28440. Epub 2013 Sep 4. Int J Cancer. 2014. PMID: 23959973

10

Molecular genetic characterization of the EWS/ATF1 fusion gene in clear cell sarcoma of tendons and aponeuroses.

Panagopoulos I, Mertens F, Dêbiec-Rychter M, Isaksson M, Limon J, Kardas I, Domanski HA, Sciot R, Perek D, Crnalic S, Larsson O, Mandahl N. Panagopoulos I, et al. Int J Cancer. 2002 Jun 1;99(4):560-7. doi: 10.1002/ijc.10404. Int J Cancer. 2002. PMID: 11992546

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