Raeymaekers P - Search Results

1

Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis.

Houwen RH, Baharloo S, Blankenship K, Raeymaekers P, Juyn J, Sandkuijl LA, Freimer NB. Houwen RH, et al. Among authors: raeymaekers p. Nat Genet. 1994 Dec;8(4):380-6. doi: 10.1038/ng1294-380. Nat Genet. 1994. PMID: 7894490

2

Linkage analysis of bipolar illness with X-chromosome DNA markers: a susceptibility gene in Xq27-q28 cannot be excluded.

De bruyn A, Raeymaekers P, Mendelbaum K, Sandkuijl LA, Raes G, Delvenne V, Hirsch D, Staner L, Mendlewicz J, Van Broeckhoven C. De bruyn A, et al. Among authors: raeymaekers p. Am J Med Genet. 1994 Dec 15;54(4):411-9. doi: 10.1002/ajmg.1320540423. Am J Med Genet. 1994. PMID: 7726217

3

Failure of familial Alzheimer's disease to segregate with the A4-amyloid gene in several European families.

Van Broeckhoven C, Genthe AM, Vandenberghe A, Horsthemke B, Backhovens H, Raeymaekers P, Van Hul W, Wehnert A, Gheuens J, Cras P, et al. Van Broeckhoven C, et al. Among authors: raeymaekers p. Nature. 1987 Sep 10-16;329(6135):153-5. doi: 10.1038/329153a0. Nature. 1987. PMID: 3306405

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

Genetic refinement and physical mapping of a chromosome 18q candidate region for bipolar disorder.

Verheyen GR, Villafuerte SM, Del-Favero J, Souery D, Mendlewicz J, Van Broeckhoven C, Raeymaekers P. Verheyen GR, et al. Among authors: raeymaekers p. Eur J Hum Genet. 1999 May-Jun;7(4):427-34. doi: 10.1038/sj.ejhg.5200318. Eur J Hum Genet. 1999. PMID: 10352933

6

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

7

A new gene (DYX3) for dyslexia is located on chromosome 2.

Fagerheim T, Raeymaekers P, Tønnessen FE, Pedersen M, Tranebjaerg L, Lubs HA. Fagerheim T, et al. Among authors: raeymaekers p. J Med Genet. 1999 Sep;36(9):664-9. J Med Genet. 1999. PMID: 10507721 Free PMC article.

8

Assignment of the Charcot-Marie-Tooth neuropathy type 1 (CMT 1a) gene to 17p11.2-p12.

Timmerman V, Raeymaekers P, De Jonghe P, De Winter G, Swerts L, Jacobs K, Gheuens J, Martin JJ, Vandenberghe A, Van Broeckhoven C. Timmerman V, et al. Among authors: raeymaekers p. Am J Hum Genet. 1990 Oct;47(4):680-5. Am J Hum Genet. 1990. PMID: 2220808 Free PMC article.

9

Homozygosity mapping to the USH2A locus in two isolated populations.

Fagerheim T, Raeymaekers P, Merren J, Mani K, Jha GK, Baumbach L, Brox V, Breines E, Holdø BE, Holdø A, Tranebjaerg L. Fagerheim T, et al. Among authors: raeymaekers p. J Med Genet. 1999 Feb;36(2):144-7. J Med Genet. 1999. PMID: 10051015 Free PMC article.

10

Linkage analysis of the Duffy blood group marker with several chromosome 1 genes in an extended pedigree with Charcot-Marie-Tooth disease.

Raeymaekers P, Van Broeckhoven C, Backhovens H, Wehnert A, Muylle L, De Jonghe P, Gheuens J, Martin JJ, Vandenberghe A. Raeymaekers P, et al. Hum Genet. 1989 Feb;81(3):231-3. doi: 10.1007/BF00278994. Hum Genet. 1989. PMID: 2921030

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