Van Roy N - Search Results

1

Identification of 2 putative critical segments of 17q gain in neuroblastoma through integrative genomics.

Vandesompele J, Michels E, De Preter K, Menten B, Schramm A, Eggert A, Ambros PF, Combaret V, Francotte N, Antonacci F, De Paepe A, Laureys G, Speleman F, Van Roy N. Vandesompele J, et al. Among authors: van roy n. Int J Cancer. 2008 Mar 1;122(5):1177-82. doi: 10.1002/ijc.23156. Int J Cancer. 2008. PMID: 17973261

2

Reciprocal translocation between the proximal regions of the long arms of chromosomes 13 and 15 resulting in unbalanced offspring: characterization by fluorescence in situ hybridization and DNA analysis.

Mangelschots K, Van Roy B, Speleman F, Van Roy N, Gheuens J, Beuten J, Buntinx I, Van Thienen MN, Willekens H, Dumon J, et al. Mangelschots K, et al. Among authors: van thienen mn, van roy b, van roy n. Hum Genet. 1992 Jun;89(4):407-13. doi: 10.1007/BF00194312. Hum Genet. 1992. PMID: 1352272

3

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

4

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

5

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

6

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

7

Molecular cytogenetic analysis of XX males using Y-specific DNA sequences, including SRY.

Van der Auwera B, Van Roy N, De Paepe A, Hawkins JR, Liebaers I, Castedo S, Dumon J, Speleman F. Van der Auwera B, et al. Among authors: van roy n. Hum Genet. 1992 Apr;89(1):23-8. doi: 10.1007/BF00207036. Hum Genet. 1992. PMID: 1577463

8

Platelet-derived growth factor A chain: confirmation of localization of PDGFA to chromosome 7p22 and description of an unusual minisatellite.

Bonthron D, Collins T, Grzeschik KH, van Roy N, Speleman F. Bonthron D, et al. Among authors: van roy n. Genomics. 1992 Jun;13(2):257-63. doi: 10.1016/0888-7543(92)90240-s. Genomics. 1992. PMID: 1612586

9

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

10

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

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