Speleman F - Search Results

1

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: speleman f. Clin Genet. 1992 Sep;42(3):105-9. doi: 10.1111/j.1399-0004.1992.tb03219.x. Clin Genet. 1992. PMID: 1395079

2

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. Clin Genet. 1992 Apr;41(4):169-74. doi: 10.1111/j.1399-0004.1992.tb03657.x. Clin Genet. 1992. PMID: 1576752

3

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. Am J Med Genet. 1991 Dec 1;41(3):381-7. doi: 10.1002/ajmg.1320410321. Am J Med Genet. 1991. PMID: 1789295

4

Molecular cytogenetic analysis of a familial pericentric inversion of chromosome 12.

Speleman F, Van Roy N, De Vos E, Hilliker C, Suijkerbuijk RF, Leroy JG. Speleman F, et al. Clin Genet. 1993 Sep;44(3):156-63. doi: 10.1111/j.1399-0004.1993.tb03869.x. Clin Genet. 1993. PMID: 8275576

5

Reassignment of MYCL1 to human chromosome 1p34.3 by fluorescence in situ hybridization.

Speleman F, Van Camp G, Van Roy N. Speleman F, et al. Cytogenet Cell Genet. 1996;72(2-3):189-90. doi: 10.1159/000134185. Cytogenet Cell Genet. 1996. PMID: 8978772

6

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: speleman f. Hum Genet. 1992 Jun;89(4):407-13. doi: 10.1007/BF00194312. Hum Genet. 1992. PMID: 1352272

7

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

8

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: speleman f. Hum Genet. 1992 Apr;89(1):23-8. doi: 10.1007/BF00207036. Hum Genet. 1992. PMID: 1577463

9

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

10

Analysis of whole-arm translocations in malignant blood cells by nonisotopic in situ hybridization.

Speleman F, Mangelschots K, Vercruyssen M, Dal Cin P, Aventin A, Offner F, Laureys G, Van den Berghe H, Leroy J. Speleman F, et al. Cytogenet Cell Genet. 1991;56(1):14-7. doi: 10.1159/000133036. Cytogenet Cell Genet. 1991. PMID: 2004549

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