Messiaen L - Search Results

1

Real-time quantitative allele discrimination assay using 3' locked nucleic acid primers for detection of low-percentage mosaic mutations.

Maertens O, Legius E, Speleman F, Messiaen L, Vandesompele J. Maertens O, et al. Among authors: messiaen l. Anal Biochem. 2006 Dec 1;359(1):144-6. doi: 10.1016/j.ab.2006.07.039. Epub 2006 Aug 14. Anal Biochem. 2006. PMID: 16962063 No abstract available.

2

Refined genetic and physical mapping of BPES type II.

Messiaen L, Leroy BP, De Bie S, De Pauw K, Van Roy N, Speleman F, Van Camp G, De Paepe A. Messiaen L, et al. Eur J Hum Genet. 1996;4(1):34-8. doi: 10.1159/000472167. Eur J Hum Genet. 1996. PMID: 8800926

3

Interstitial deletion 2q33.3-q34 in a boy with a phenotype resembling the Seckel syndrome.

Courtens W, Speleman F, Messiaen L, Bormans J, Van Roy N, Vamos E. Courtens W, et al. Among authors: messiaen l. Am J Med Genet. 1997 Sep 5;71(4):479-85. Am J Med Genet. 1997. PMID: 9286460 Review.

4

Molecular analysis of 1p36 breakpoints in two Merkel cell carcinomas.

Van Gele M, Van Roy N, Ronan SG, Messiaen L, Vandesompele J, Geerts ML, Naeyaert JM, Blennow E, Bar-Am I, Das Gupta TK, van der Drift P, Versteeg R, Leonard JH, Speleman F. Van Gele M, et al. Among authors: messiaen l. Genes Chromosomes Cancer. 1998 Sep;23(1):67-71. doi: 10.1002/(sici)1098-2264(199809)23:1<67::aid-gcc10>3.0.co;2-b. Genes Chromosomes Cancer. 1998. PMID: 9713999

5

Noonan-like phenotype in monozygotic twins with a duplication-deficiency of the long arm of chromosome 18 resulting from a maternal paracentric inversion.

Courtens W, Grossman D, Van Roy N, Messiaen L, Vamos E, Toppet V, Haumont D, Streydio C, Jauch A, Vermeesch JR, Speleman F. Courtens W, et al. Among authors: messiaen l. Hum Genet. 1998 Oct;103(4):497-505. doi: 10.1007/s004390050857. Hum Genet. 1998. PMID: 9856497

6

Assignment of the cellular retinol-binding protein 1 gene (RBP1) and of the coatomer beta subunit gene (COPB2) to human chromosome band 3q23 by in situ hybridization.

De Baere E, Speleman F, Van Roy N, De Paepe A, Messiaen L. De Baere E, et al. Among authors: messiaen l. Cytogenet Cell Genet. 1998;82(3-4):226-7. doi: 10.1159/000015107. Cytogenet Cell Genet. 1998. PMID: 9858824 No abstract available.

7

Assignment of SHOX2 (alias OG12X and SHOT) to human chromosome bands 3q25-->q26.1 by in situ hybridization.

De Baere E, Speleman F, Van Roy N, De Paepe A, Messiaen L. De Baere E, et al. Among authors: messiaen l. Cytogenet Cell Genet. 1998;82(3-4):228-9. doi: 10.1159/000015108. Cytogenet Cell Genet. 1998. PMID: 9858825 No abstract available.

8

Assignment of the cellular retinol-binding protein 2 gene (RBP2) to human chromosome band 3q23 by in situ hybridization.

De Baere E, Speleman F, Van Roy N, Mortier K, De Paepe A, Messiaen L. De Baere E, et al. Among authors: messiaen l. Cytogenet Cell Genet. 1998;83(3-4):240-1. doi: 10.1159/000015191. Cytogenet Cell Genet. 1998. PMID: 10072590 No abstract available.

9

Closing in on the BPES gene on 3q23: mapping of a de Novo reciprocal translocation t(3;4)(q23;p15.2) breakpoint within a 45-kb cosmid and mapping of three candidate genes, RBP1, RBP2, and beta'-COP, distal to the breakpoint.

De Baere E, Van Roy N, Speleman F, Fukushima Y, De Paepe A, Messiaen L. De Baere E, et al. Among authors: messiaen l. Genomics. 1999 Apr 1;57(1):70-8. doi: 10.1006/geno.1999.5747. Genomics. 1999. PMID: 10191085

10

Exhaustive mutation analysis of the NF1 gene allows identification of 95% of mutations and reveals a high frequency of unusual splicing defects.

Messiaen LM, Callens T, Mortier G, Beysen D, Vandenbroucke I, Van Roy N, Speleman F, Paepe AD. Messiaen LM, et al. Hum Mutat. 2000;15(6):541-55. doi: 10.1002/1098-1004(200006)15:6<541::AID-HUMU6>3.0.CO;2-N. Hum Mutat. 2000. PMID: 10862084

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