Speleman F - Search Results

1

Improved immunocytochemical detection of biotinylated probes with Neutralite avidin.

van Roy N, Mangelschots K, Speleman F. van Roy N, et al. Among authors: speleman f. Trends Genet. 1993 Mar;9(3):71-2. doi: 10.1016/0168-9525(93)90217-6. Trends Genet. 1993. PMID: 8488564 No abstract available.

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 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

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

5

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

6

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

7

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

8

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

9

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

10

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

412 results

Search Page

Filters