Van Roy N - Search Results

1

Isolation of disseminated neuroblastoma cells from bone marrow aspirates for pretreatment risk assessment by array comparative genomic hybridization.

Vandewoestyne M, Kumps C, Swerts K, Menten B, Lammens T, Philippé J, De Preter K, Laureys G, Van Roy N, Speleman F, Deforce D. Vandewoestyne M, et al. Among authors: van roy n. Int J Cancer. 2012 Mar 1;130(5):1098-108. doi: 10.1002/ijc.26133. Epub 2011 Jun 9. Int J Cancer. 2012. PMID: 21484798

2

Molecular cytogenetic analysis of a complex t(10;22;11) translocation in Ewing's sarcoma.

Speleman F, Van Roy N, Wiegant J, Dierick AM, Uyttendaele D, Leroy JG. Speleman F, et al. Among authors: van roy n. Genes Chromosomes Cancer. 1992 Mar;4(2):188-91. doi: 10.1002/gcc.2870040214. Genes Chromosomes Cancer. 1992. PMID: 1373321

3

Uterine leiomyoma cytogenetics. III. Interphase cytogenetic analysis of karyotypically normal uterine leiomyoma excludes possibility of undetected trisomy 12.

Vanni R, Van Roy N, Lecca U, Speleman F. Vanni R, et al. Among authors: van roy n. Cancer Genet Cytogenet. 1992 Aug;62(1):40-2. doi: 10.1016/0165-4608(92)90035-7. Cancer Genet Cytogenet. 1992. PMID: 1521231

4

Detection of subtle reciprocal translocations by fluorescence in situ hybridization.

Speleman F, Van Roy N, Wiegant J, Verschraegen-Spae MR, Benoit Y, Govaert P, Goossens L, Leroy JG. Speleman F, et al. Among authors: van roy n. Clin Genet. 1992 Apr;41(4):169-74. doi: 10.1111/j.1399-0004.1992.tb03657.x. Clin Genet. 1992. PMID: 1576752

5

Pallister-Killian syndrome: characterization of the isochromosome 12p by fluorescent in situ hybridization.

Speleman F, Leroy JG, Van Roy N, De Paepe A, Suijkerbuijk R, Brunner H, Looijenga L, Verschraegen-Spae MR, Orye E. Speleman F, et al. Among authors: van roy n. Am J Med Genet. 1991 Dec 1;41(3):381-7. doi: 10.1002/ajmg.1320410321. Am J Med Genet. 1991. PMID: 1789295

6

Is t(6;20)(p21;q13) a characteristic chromosome change in endometrial polyps?

Speleman F, Dal Cin P, Van Roy N, Van Marck E, Buytaert P, Van den Berghe H, Leroy JG. Speleman F, et al. Among authors: van marck e, van den berghe h, van roy n. Genes Chromosomes Cancer. 1991 Jul;3(4):318-9. doi: 10.1002/gcc.2870030412. Genes Chromosomes Cancer. 1991. PMID: 1958597

7

1;17 translocations and other chromosome 17 rearrangements in human primary neuroblastoma tumors and cell lines.

Van Roy N, Laureys G, Cheng NC, Willem P, Opdenakker G, Versteeg R, Speleman F. Van Roy N, et al. Genes Chromosomes Cancer. 1994 Jun;10(2):103-14. doi: 10.1002/gcc.2870100205. Genes Chromosomes Cancer. 1994. PMID: 7520263

8

Characterisation of the chromosome breakpoints in a patient with a constitutional translocation t(1;17)(p36.31-p36.13;q11.2-q12) and neuroblastoma.

Laureys G, Versteeg R, Speleman F, van der Drift P, Francke U, Opdenakker G, Van Roy N. Laureys G, et al. Among authors: van der drift p, van roy n. Eur J Cancer. 1995;31A(4):523-6. doi: 10.1016/0959-8049(95)00012-8. Eur J Cancer. 1995. PMID: 7576958

9

Molecular cytogenetic analysis of 1;17 translocations in neuroblastoma.

Van Roy N, Cheng NC, Laureys G, Opdenakker G, Versteeg R, Speleman F. Van Roy N, et al. Eur J Cancer. 1995;31A(4):530-5. doi: 10.1016/0959-8049(95)00004-3. Eur J Cancer. 1995. PMID: 7576960

10

Identification of two distinct chromosome 12-derived amplification units in neuroblastoma cell line NGP.

Van Roy N, Forus A, Myklebost O, Cheng NC, Versteeg R, Speleman F. Van Roy N, et al. Cancer Genet Cytogenet. 1995 Jul 15;82(2):151-4. doi: 10.1016/0165-4608(95)00034-m. Cancer Genet Cytogenet. 1995. PMID: 7664245

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