Van Roy N - Search Results

1

Genome dynamics of the human embryonic kidney 293 lineage in response to cell biology manipulations.

Lin YC, Boone M, Meuris L, Lemmens I, Van Roy N, Soete A, Reumers J, Moisse M, Plaisance S, Drmanac R, Chen J, Speleman F, Lambrechts D, Van de Peer Y, Tavernier J, Callewaert N. Lin YC, et al. Among authors: van de peer y, van roy n. Nat Commun. 2014 Sep 3;5:4767. doi: 10.1038/ncomms5767. Nat Commun. 2014. PMID: 25182477 Free PMC article.

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

Putative monosomy 21 in two patients: clinical findings and investigation using fluorescence in situ hybridization.

Viljoen DL, Speleman F, Smart R, Van Roy N, du Toit J, Leroy J. Viljoen DL, et al. Among authors: van roy n. Clin Genet. 1992 Sep;42(3):105-9. doi: 10.1111/j.1399-0004.1992.tb03219.x. Clin Genet. 1992. PMID: 1395079

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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