Speleman F - Search Results

1

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

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

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

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

Familial Turner syndrome.

Verschraegen-Spae MR, Depypere H, Speleman F, Dhondt M, De Paepe A. Verschraegen-Spae MR, et al. Among authors: speleman f. Clin Genet. 1992 Apr;41(4):218-20. doi: 10.1111/j.1399-0004.1992.tb03666.x. Clin Genet. 1992. PMID: 1576760

6

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

7

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.

8

Proximal deletion of chromosome 21 confirmed by in situ hybridization and molecular studies.

Courtens W, Petersen MB, Noël JC, Flament-Durand J, Van Regemorter N, Delneste D, Cochaux P, Verschraegen-Spae MR, Van Roy N, Speleman F, et al. Courtens W, et al. Among authors: speleman f. Am J Med Genet. 1994 Jul 1;51(3):260-5. doi: 10.1002/ajmg.1320510318. Am J Med Genet. 1994. PMID: 8074156 Review.

9

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

10

Molecular cytogenetic characterization of marker chromosomes found at prenatal diagnosis.

Verschraegen-Spae MR, van Roy N, de Perdigo A, de Paepe A, Speleman F. Verschraegen-Spae MR, et al. Among authors: speleman f. Prenat Diagn. 1993 May;13(5):385-94. doi: 10.1002/pd.1970130511. Prenat Diagn. 1993. PMID: 8341637

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