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European Journal of Human Genetics : EJHG|January 1, 1996
Phenylalanine hydroxylase gene mutation R408W is present on 84% of Estonian phenylketonuria chromosomesH Lilleväli, K Ounap, A Metspalu
European Journal of Human Genetics : EJHG|January 1, 1996
Arylsulfatase A pseudodeficiency--incidence in PolandB Czartoryska, J G Zimowski, M Bisko, et al.
European Journal of Human Genetics : EJHG|January 1, 1995
A limited genomic region contains the human REG and REG-related genesC Bartoli, J C Dagorn, M Fontes, et al.
European Journal of Human Genetics : EJHG|January 1, 1995
Molecular genetics of the human chondrodysplasias-1995W A Horton
European Journal of Human Genetics : EJHG|January 1, 1996
Population genetic comparisons among eight populations using allele frequency and sequence data from three microsatellite lociB Brinkmann, A Sajantila, H W Goedde, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative studyE Nelis, C Van Broeckhoven, P De Jonghe, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Refined genetic and physical mapping of BPES type IIL Messiaen, B P Leroy, S De Bie, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Gly802Asp substitution in the pro alpha 2(I) collagen chain in a family with recurrent osteogenesis imperfecta due to paternal mosaicismA M Lund, M Schwartz, M Raghunath, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Types I and III Gaucher disease in Poland: incidence of the most common mutations and phenotypic manifestationsA Tylki-Szymańska, G Millat, I Maire, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Cystic fibrosis heterozygote screening in the Orthodox Community of Ashkenazi Jews: the Dor Yesharim approach and heterozygote frequencyD Abeliovich, A Quint, N Weinberg, et al.
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