Messiaen L - Search Results

1

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

2

An interstitial deletion of chromosome 7 at band q21: a case report and review.

Courtens W, Vermeulen S, Wuyts W, Messiaen L, Wauters J, Nuytinck L, Peeters N, Storm K, Speleman F, Nöthen MM. Courtens W, et al. Among authors: messiaen l. Am J Med Genet A. 2005 Apr 1;134A(1):12-23. doi: 10.1002/ajmg.a.30106. Am J Med Genet A. 2005. PMID: 15732063 Review.

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

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

5

Familial pericentric inversion of chromosome 18: behavioral abnormalities in patients heterozygous for either the dup(18p)/del(18q) or dup(18q)/del(18p) recombinant chromosome.

Vermeulen SJ, Speleman F, Vanransbeeck L, Verspeet J, Menten B, Verschraegen-Spae MR, Wilde PD, Messiaen L, Michaelis RC, Leroy JG. Vermeulen SJ, et al. Among authors: messiaen l. Eur J Hum Genet. 2005 Jan;13(1):52-8. doi: 10.1038/sj.ejhg.5201281. Eur J Hum Genet. 2005. PMID: 15470365

6

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

7

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

8

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.

9

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.

10

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.

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