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European Journal of Human Genetics : EJHG|November 26, 1999
A common disease haplotype segregating in spinocerebellar ataxia 2 (SCA2) pedigrees of diverse ethnic originJ Pang, R Allotey, N Wadia, et al.
European Journal of Human Genetics : EJHG|April 10, 1999
Mutation in the zonadhesin-like domain of alpha-tectorin associated with autosomal dominant non-syndromic hearing lossN Alloisio, L Morlé, M Bozon, et al.
European Journal of Human Genetics : EJHG|May 11, 1999
A novel locus for Usher syndrome type II, USH2B, maps to chromosome 3 at p23-24.2M Hmani, A Ghorbel, A Boulila-Elgaied, et al.
European Journal of Human Genetics : EJHG|May 11, 1999
Three widespread founder mutations contribute to high incidence of X-linked juvenile retinoschisis in FinlandL Huopaniemi, A Rantala, H Forsius, et al.
European Journal of Human Genetics : EJHG|March 27, 1999
An integrated map of chromosome 18 CAG trinucleotide repeat lociA J Grierson, M van Groenigen, N P Groot, et al.
European Journal of Human Genetics : EJHG|March 27, 1999
Novel mutations in Rsk-2, the gene for Coffin-Lowry syndrome (CLS)F Abidi, S Jacquot, C Lassiter, et al.
European Journal of Human Genetics : EJHG|March 27, 1999
Heterogeneous spectrum of mutations in the Fanconi anaemia group A geneM Wijker, N V Morgan, S Herterich, et al.
European Journal of Human Genetics : EJHG|March 27, 1999
Spectrum of mutations in fucosidosisP J Willems, H C Seo, P Coucke, et al.
European Journal of Human Genetics : EJHG|January 1, 1995
Expression of the human Dp 71 (apo-dystrophin-1) gene from a 760-kb DMD-YAC transferred to mouse cellsJ C Heikoop, F B Hogervorst, E J Meershoek, et al.
European Journal of Human Genetics : EJHG|January 1, 1995
Convergent myotonic dystrophy (DM) haplotypes: potential inconsistencies in human disease gene localizationE J Whiting, C Tsilfidis, L Surh, et al.
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