Messiaen L - Search Results

1

Does monosymptomatic enuresis exist? A molecular genetic exploration of 32 families with enuresis/incontinence.

Loeys B, Hoebeke P, Raes A, Messiaen L, De Paepe A, Vande Walle J. Loeys B, et al. Among authors: messiaen l. BJU Int. 2002 Jul;90(1):76-83. doi: 10.1046/j.1464-410x.2002.02775.x. BJU Int. 2002. PMID: 12081775

2

Kallmann syndrome in a patient with congenital spherocytosis and an interstitial 8p11.2 deletion.

Vermeulen S, Messiaen L, Scheir P, De Bie S, Speleman F, De Paepe A. Vermeulen S, et al. Among authors: messiaen l. Am J Med Genet. 2002 Apr 1;108(4):315-8. doi: 10.1002/ajmg.10295. Am J Med Genet. 2002. PMID: 11920837

3

Strategies for prenatal and preimplantation genetic diagnosis in Marfan syndrome (MFS).

Loeys B, Nuytinck L, Van Acker P, Walraedt S, Bonduelle M, Sermon K, Hamel B, Sanchez A, Messiaen L, De Paepe A. Loeys B, et al. Among authors: messiaen l. Prenat Diagn. 2002 Jan;22(1):22-8. Prenat Diagn. 2002. PMID: 11810645

4

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.

5

The human FOXL2 mutation database.

Beysen D, Vandesompele J, Messiaen L, De Paepe A, De Baere E. Beysen D, et al. Among authors: messiaen l. Hum Mutat. 2004 Sep;24(3):189-93. doi: 10.1002/humu.20079. Hum Mutat. 2004. PMID: 15300845

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

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

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

Evidence for involvement of a tumor suppressor gene on 1p in malignant peripheral nerve sheath tumors.

Van Roy N, Van Gele M, Vandesompele J, Messiaen L, Van Belle S, Sciot R, Mortéle K, Gyselinck J, Michiels E, Forsyth R, Van Marck E, De Paepe A, Speleman F. Van Roy N, et al. Among authors: messiaen l. Cancer Genet Cytogenet. 2003 Jun;143(2):120-4. doi: 10.1016/s0165-4608(02)00853-1. Cancer Genet Cytogenet. 2003. PMID: 12781445

10

Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome.

Beysen D, Raes J, Leroy BP, Lucassen A, Yates JR, Clayton-Smith J, Ilyina H, Brooks SS, Christin-Maitre S, Fellous M, Fryns JP, Kim JR, Lapunzina P, Lemyre E, Meire F, Messiaen LM, Oley C, Splitt M, Thomson J, Van de Peer Y, Veitia RA, De Paepe A, De Baere E. Beysen D, et al. Among authors: messiaen lm. Am J Hum Genet. 2005 Aug;77(2):205-18. doi: 10.1086/432083. Epub 2005 Jun 16. Am J Hum Genet. 2005. PMID: 15962237 Free PMC article.

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 NCBI Filters

Text availability

Article attribute

Article type

Publication date

185 results

Search Page