Claes S - Search Results

1

X linked mental retardation and infantile spasms in a family: new clinical data and linkage to Xp11.4-Xp22.11.

Strømme P, Sundet K, Mørk C, Cassiman JJ, Fryns JP, Claes S. Strømme P, et al. Among authors: claes s. J Med Genet. 1999 May;36(5):374-8. J Med Genet. 1999. PMID: 10353782 Free PMC article.

2

Linkage analysis in three families with nonspecific X-linked mental retardation.

Claes S, Gu XX, Legius E, Lorenzetti E, Marynen P, Fryns JP, Cassiman JJ, Raeymaekers P. Claes S, et al. Am J Med Genet. 1996 Jul 12;64(1):137-46. doi: 10.1002/(SICI)1096-8628(19960712)64:1<137::AID-AJMG24>3.0.CO;2-N. Am J Med Genet. 1996. PMID: 8826464

3

X-linked severe mental retardation and a progressive neurological disorder in a Belgian family: clinical and genetic studies.

Claes S, Devriendt K, D'Adamo P, Meireleire J, Raeymaekers P, Toniolo D, Cassiman JJ, Fryns JP. Claes S, et al. Clin Genet. 1997 Sep;52(3):155-61. doi: 10.1111/j.1399-0004.1997.tb02536.x. Clin Genet. 1997. PMID: 9377804

4

Regional localization of two genes for nonspecific X-linked mental retardation to Xp22.3-p22.2 (MRX49) and Xp11.3-p11.21 (MRX50).

Claes S, Vogels A, Holvoet M, Devriendt K, Raeymaekers P, Cassiman JJ, Fryns JP. Claes S, et al. Am J Med Genet. 1997 Dec 31;73(4):474-9. Am J Med Genet. 1997. PMID: 9415477

5

Regional localization of a gene for nonspecific XLMR to Xp11.3-p11. 23 (MRX51) and tentative localization of an MRX gene to Xq23-q26.1.

Claes S, Volcke P, Devriendt K, Holvoet M, Raeymaekers P, Cassiman JJ, Fryns JP. Claes S, et al. Am J Med Genet. 1999 Jul 30;85(3):283-7. Am J Med Genet. 1999. PMID: 10398244

6

Novel syndromic form of X-linked complicated spastic paraplegia.

Claes S, Devriendt K, Van Goethem G, Roelen L, Meireleire J, Raeymaekers P, Cassiman JJ, Fryns JP. Claes S, et al. Am J Med Genet. 2000 Sep 4;94(1):1-4. doi: 10.1002/1096-8628(20000904)94:1<1::aid-ajmg1>3.0.co;2-v. Am J Med Genet. 2000. PMID: 10982473

7

The X-linked infantile spasms syndrome (MIM 308350) maps to Xp11.4-Xpter in two pedigrees.

Claes S, Devriendt K, Lagae L, Ceulemans B, Dom L, Casaer P, Raeymaekers P, Cassiman JJ, Fryns JP. Claes S, et al. Ann Neurol. 1997 Sep;42(3):360-4. doi: 10.1002/ana.410420313. Ann Neurol. 1997. PMID: 9307258

8

X-linked nonspecific mental retardation (MRX) linkage studies in 25 unrelated families: the European XLMR consortium.

des Portes V, Beldjord C, Chelly J, Hamel B, Kremer H, Smits A, van Bokhoven H, Ropers HH, Claes S, Fryns JP, Ronce N, Gendrot C, Toutain A, Raynaud M, Moraine C. des Portes V, et al. Among authors: claes s. Am J Med Genet. 1999 Jul 30;85(3):263-5. doi: 10.1002/(sici)1096-8628(19990730)85:3<263::aid-ajmg15>3.0.co;2-0. Am J Med Genet. 1999. PMID: 10398240 No abstract available.

9

Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysis.

Devriendt K, Matthijs G, Claes S, Legius E, Proesmans W, Cassiman JJ, Fryns JP. Devriendt K, et al. Among authors: claes s. J Med Genet. 1997 Apr;34(4):318-22. doi: 10.1136/jmg.34.4.318. J Med Genet. 1997. PMID: 9138157 Free PMC article.

10

Non-syndromic deafness associated with a mutation and a polymorphism in the mitochondrial 12S ribosomal RNA gene in a large Zairean pedigree.

Matthijs G, Claes S, Longo-Mbenza B, Cassiman JJ. Matthijs G, et al. Among authors: claes s. Eur J Hum Genet. 1996;4(1):46-51. doi: 10.1159/000472169. Eur J Hum Genet. 1996. PMID: 8800928

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

288 results

Search Page