Raeymaekers P - Search Results

1

Identification of a new locus for autosomal dominant non-syndromic hearing impairment (DFNA7) in a large Norwegian family.

Fagerheim T, Nilssen O, Raeymaekers P, Brox V, Moum T, Elverland HH, Teig E, Omland HH, Fostad GK, Tranebjaerg L. Fagerheim T, et al. Among authors: raeymaekers p. Hum Mol Genet. 1996 Aug;5(8):1187-91. doi: 10.1093/hmg/5.8.1187. Hum Mol Genet. 1996. PMID: 8842739

2

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.

3

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.

4

Further localization of X-linked hydrocephalus in the chromosomal region Xq28.

Willems PJ, Vits L, Raeymaekers P, Beuten J, Coucke P, Holden JJ, Van Broeckhoven C, Warren ST, Sagi M, Robinson D, et al. Willems PJ, et al. Among authors: raeymaekers p. Am J Hum Genet. 1992 Aug;51(2):307-15. Am J Hum Genet. 1992. PMID: 1642232 Free PMC article.

5

X-linked liver glycogenosis: localization and isolation of a candidate gene.

Hendrickx J, Coucke P, Bossuyt P, Wauters J, Raeymaekers P, Marchau F, Smit GP, Stolte I, Sardharwalla IB, Berthelot J, et al. Hendrickx J, et al. Among authors: raeymaekers p. Hum Mol Genet. 1993 May;2(5):583-9. doi: 10.1093/hmg/2.5.583. Hum Mol Genet. 1993. PMID: 8518797

6

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

7

The Duffy blood group is linked to the alpha-spectrin locus in a large pedigree with autosomal dominant inheritance of Charcot-Marie-Tooth disease type 1.

Raeymaekers P, Van Broeckhoven C, Backhovens H, Wehnert A, Muylle L, De Jonghe P, Gheuens J, Vandenberghe A. Raeymaekers P, et al. Hum Genet. 1988 Jan;78(1):76-8. doi: 10.1007/BF00291239. Hum Genet. 1988. PMID: 2892777

8

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

9

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

10

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

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