Raeymaekers P - Search Results

1

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

2

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

3

Lack of association between HLA class II polymorphisms and essential hypertension in a Belgian population.

Gu XX, Spaepen M, Raeymaekers P, Guo C, Fagard R, Amery A, Lijnen P, Cassiman JJ. Gu XX, et al. Among authors: raeymaekers p. J Hum Hypertens. 1995 Jul;9(7):553-5. J Hum Hypertens. 1995. PMID: 7562884

4

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.

5

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

6

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.

7

A chromosome 18 genetic linkage study in three large Belgian pedigrees with bipolar disorder.

Claes S, Raeymaekers P, Van den Broeck M, Diependaele S, De bruyn A, Verheyen G, Wils V, Boogaerts A, Tanghe A, Godderis J, Van Broeckhoven C, Cassiman JJ. Claes S, et al. Among authors: raeymaekers p. J Affect Disord. 1997 May;43(3):195-205. doi: 10.1016/s0165-0327(97)01429-8. J Affect Disord. 1997. PMID: 9186790

8

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. Among authors: raeymaekers p. Ann Neurol. 1997 Sep;42(3):360-4. doi: 10.1002/ana.410420313. Ann Neurol. 1997. PMID: 9307258

9

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

10

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

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