Raeymaekers P - Search Results

1

Localisation of a new gene for non-specific mental retardation to Xq22-q26 (MRX35).

Gu XX, Decorte R, Marynen P, Fryns JP, Cassiman JJ, Raeymaekers P. Gu XX, et al. Among authors: raeymaekers p. J Med Genet. 1996 Jan;33(1):52-5. doi: 10.1136/jmg.33.1.52. J Med Genet. 1996. PMID: 8825049 Free PMC article.

2

Linkage of type I diabetes to 15q26 (IDDM3) in the Danish population.

Zamani M, Pociot F, Raeymaekers P, Nerup J, Cassiman JJ. Zamani M, et al. Among authors: raeymaekers p. Hum Genet. 1996 Oct;98(4):491-6. doi: 10.1007/s004390050245. Hum Genet. 1996. PMID: 8792828

3

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. Among authors: raeymaekers p. 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

4

Linkage and association of the HLA gene complex with IDDM in 81 Danish families: strong linkage between DR beta 1Lys71+ and IDDM.

Zamani M, Pociot F, Spaepen M, Raeymaekers P, Nerup J, Cassiman JJ. Zamani M, et al. Among authors: raeymaekers p. J Med Genet. 1996 Nov;33(11):899-905. doi: 10.1136/jmg.33.11.899. J Med Genet. 1996. PMID: 8950668 Free PMC article.

5

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. Among authors: raeymaekers p. Clin Genet. 1997 Sep;52(3):155-61. doi: 10.1111/j.1399-0004.1997.tb02536.x. Clin Genet. 1997. PMID: 9377804

6

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. Among authors: raeymaekers p. Am J Med Genet. 1997 Dec 31;73(4):474-9. Am J Med Genet. 1997. PMID: 9415477

7

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. Among authors: raeymaekers p. Am J Med Genet. 1999 Jul 30;85(3):283-7. Am J Med Genet. 1999. PMID: 10398244

8

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. Among authors: raeymaekers p. 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

9

CFTR haplotype backgrounds on normal and mutant CFTR genes.

Cuppens H, Teng H, Raeymaekers P, De Boeck C, Cassiman JJ. Cuppens H, et al. Among authors: raeymaekers p. Hum Mol Genet. 1994 Apr;3(4):607-14. doi: 10.1093/hmg/3.4.607. Hum Mol Genet. 1994. PMID: 7520797

10

A radiation hybrid map with 60 loci covering the entire short arm of chromosome 12.

Raeymaekers P, Van Zand K, Jun L, Höglund M, Cassiman JJ, Van den Berghe H, Marynen P. Raeymaekers P, et al. Genomics. 1995 Sep 1;29(1):170-8. doi: 10.1006/geno.1995.1228. Genomics. 1995. PMID: 8530068

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