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European Journal of Human Genetics : EJHG|October 22, 1998
BRCA2 germline mutations in Swedish breast cancer familiesJ Chen, M Z Hedman, B W Arver, et al.European Journal of Human Genetics : EJHG|October 22, 1998
Lower frequency of Gaucher disease carriers among Tay-Sachs disease carriersL Peleg, A Frisch, B Goldman, et al.European Journal of Human Genetics : EJHG|January 26, 2006
Y-chromosomal STR haplotype analysis reveals surname-associated strata in the East-German populationUta-Dorothee Immel, Michael Krawczak, Jürgen Udolph, et al.European Journal of Human Genetics : EJHG|January 19, 2006
Mutation screening in patients with syndromic craniosynostoses indicates that a limited number of recurrent FGFR2 mutations accounts for severe forms of Pfeiffer syndromeElisabeth Lajeunie, Solange Heuertz, Vincent El Ghouzzi, et al.European Journal of Human Genetics : EJHG|January 1, 1997
Prenatal diagnosis in BelgiumE Vamos, K Vandenberghe, J J CassimanEuropean Journal of Human Genetics : EJHG|January 1, 1997
Prenatal diagnosis services in GreeceC Metaxotou, A Mavrou, A AntasaklisEuropean Journal of Human Genetics : EJHG|January 1, 1997
Prenatal diagnosis in LuxembourgF C SchneiderEuropean Journal of Human Genetics : EJHG|January 1, 1996
Assignment of genes coding for brown eye colour (BEY2) and brown hair colour (HCL3) on chromosome 15qH Eiberg, J MohrEuropean Journal of Human Genetics : EJHG|January 1, 1996
Clinical heterogeneity in 16 patients with inv dup 15 chromosome: cytogenetic and molecular studies, search for an imprinting effectC Mignon, P Malzac, A Moncla, et al.European Journal of Human Genetics : EJHG|January 1, 1996
Audit of maternal serum screening: strategies to augment counselling in response to women's viewsJ Burn, S Fairgrieve, P Franks, et al.Pageof 563