Speleman F - Search Results

1

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. Among authors: speleman f. Genes Chromosomes Cancer. 1994 Jun;10(2):103-14. doi: 10.1002/gcc.2870100205. Genes Chromosomes Cancer. 1994. PMID: 7520263

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. Genes Chromosomes Cancer. 1992 Mar;4(2):188-91. doi: 10.1002/gcc.2870040214. Genes Chromosomes Cancer. 1992. PMID: 1373321

3

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. Genes Chromosomes Cancer. 1991 Jul;3(4):318-9. doi: 10.1002/gcc.2870030412. Genes Chromosomes Cancer. 1991. PMID: 1958597

4

Constitutional translocation t(1;17)(p36;q12-21) in a patient with neuroblastoma.

Laureys G, Speleman F, Opdenakker G, Benoit Y, Leroy J. Laureys G, et al. Among authors: speleman f. Genes Chromosomes Cancer. 1990 Sep;2(3):252-4. doi: 10.1002/gcc.2870020315. Genes Chromosomes Cancer. 1990. PMID: 2078517

5

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: speleman f. Eur J Cancer. 1995;31A(4):523-6. doi: 10.1016/0959-8049(95)00012-8. Eur J Cancer. 1995. PMID: 7576958

6

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. Among authors: speleman f. Eur J Cancer. 1995;31A(4):530-5. doi: 10.1016/0959-8049(95)00004-3. Eur J Cancer. 1995. PMID: 7576960

7

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. Among authors: speleman f. Cancer Genet Cytogenet. 1995 Jul 15;82(2):151-4. doi: 10.1016/0165-4608(95)00034-m. Cancer Genet Cytogenet. 1995. PMID: 7664245

8

Constitutional translocation t(1;17)(p36.31-p36.13;q11.2-q12.1) in a neuroblastoma patient. Establishment of somatic cell hybrids and identification of PND/A12M2 on chromosome 1 and NF1/SCYA7 on chromosome 17 as breakpoint flanking single copy markers.

Laureys G, Speleman F, Versteeg R, van der Drift P, Chan A, Leroy J, Francke U, Opdenakker G, Van Roy N. Laureys G, et al. Among authors: speleman f. Oncogene. 1995 Mar 16;10(6):1087-93. Oncogene. 1995. PMID: 7700633

9

Deletion mapping in neuroblastoma cell lines suggests two distinct tumor suppressor genes in the 1p35-36 region, only one of which is associated with N-myc amplification.

Cheng NC, Van Roy N, Chan A, Beitsma M, Westerveld A, Speleman F, Versteeg R. Cheng NC, et al. Among authors: speleman f. Oncogene. 1995 Jan 19;10(2):291-7. Oncogene. 1995. PMID: 7838528

10

High-resolution fluorescence mapping of 46 DNA markers to the short arm of human chromosome 1.

Van Roy N, Laureys G, Versteeg R, Opdenakker G, Speleman F. Van Roy N, et al. Among authors: speleman f. Genomics. 1993 Oct;18(1):71-8. doi: 10.1006/geno.1993.1427. Genomics. 1993. PMID: 8276418

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