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European Journal of Human Genetics : EJHG|February 24, 2006
Extreme heterogeneity in CARD15 and DLG5 Crohn disease-associated polymorphisms between German and Norwegian populationsValentina Medici, Silvia Mascheretti, Peter J P Croucher, et al.
European Journal of Human Genetics : EJHG|January 15, 1999
Genetic linkage of Meleda disease to chromosome 8qterJ Fischer, B Bouadjar, R Heilig, et al.
European Journal of Human Genetics : EJHG|January 15, 1999
Genetic mapping of X-linked loci involved in skewing of X chromosome inactivation in the humanA K Naumova, L Olien, L M Bird, et al.
European Journal of Human Genetics : EJHG|January 15, 1999
Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutationS Abe, S Usami, H Shinkawa, et al.
European Journal of Human Genetics : EJHG|January 15, 1999
X-linked ocular albinism: prevalence and mutations--a national studyT Rosenberg, M Schwartz
European Journal of Human Genetics : EJHG|January 15, 1999
Strong founder effect for a transglutaminase 1 gene mutation in lamellar ichthyosis and congenital ichthyosiform erythroderma from NorwayM Pigg, T Gedde-Dahl, D Cox, et al.
European Journal of Human Genetics : EJHG|January 15, 1999
Different ancestor alleles: a reason for the bimodal fragment size distribution in the minisatellite D2S44 (YNH24)G Holmlund, B Lindblom
European Journal of Human Genetics : EJHG|January 15, 1999
His1069Gln and six novel Wilson disease mutations: analysis of relevance for early diagnosis and phenotypeH H Duc, H Hefter, W Stremmel, et al.
European Journal of Human Genetics : EJHG|January 15, 1999
Endemic Tyrolean infantile cirrhosis is not an allelic variant of Wilson's diseaseC Wijmenga, T Müller, I S Murli, et al.
European Journal of Human Genetics : EJHG|January 15, 1999
Exclusion of the SCN2B gene as candidate for CMT4BA Bolino, M Seri, F Caroli, et al.
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