Speleman F - Search Results

1

Identification and characterization of normal length nonfluorescent Y chromosomes: cytogenetic analysis, southern hybridization and non-isotopic in situ hybridization.

Speleman F, Van der Auwera B, Mangelschots K, Vercruyssen M, Raap T, Wiegant J, Craen M, Leroy J. Speleman F, et al. Hum Genet. 1990 Oct;85(6):569-75. doi: 10.1007/BF00193576. Hum Genet. 1990. PMID: 2227946

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

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

5

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

6

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

7

Characterization of a de novo duplication of 11p14----p13, using fluorescent in situ hybridization and southern hybridization.

Speleman F, Mannens M, Redeker B, Vercruyssen M, Van Oostveldt P, Leroy J, Slater R. Speleman F, et al. Cytogenet Cell Genet. 1991;56(3-4):129-31. doi: 10.1159/000133068. Cytogenet Cell Genet. 1991. PMID: 2055105

8

De novo terminal deletion 7p22.1--pter in a child without craniosynostosis.

Speleman F, Craen M, Leroy J. Speleman F, et al. J Med Genet. 1989 Aug;26(8):528-32. doi: 10.1136/jmg.26.8.528. J Med Genet. 1989. PMID: 2671374 Free PMC article. Review.

9

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

10

Malignant melanoma of soft parts. Further cytogenetic characterization.

Speleman F, Colpaert C, Goovaerts G, Leroy JG, Van Marck E. Speleman F, et al. Cancer Genet Cytogenet. 1992 Jun;60(2):176-9. doi: 10.1016/0165-4608(92)90012-w. Cancer Genet Cytogenet. 1992. PMID: 1606560

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