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European Journal of Human Genetics : EJHG|April 29, 2020
Cognitive and affective outcomes of genetic counselling in the Netherlands at group and individual level: a personalized approach seems necessaryJan S Voorwinden, Mirjam Plantinga, Margreet Ausems, et al.
European Journal of Human Genetics : EJHG|June 3, 2020
Attitudes of relatives of mucopolysaccharidosis type III patients toward preconception expanded carrier screeningStephanie C M Nijmeijer, Thirsa Conijn, Phillis Lakeman, et al.
European Journal of Human Genetics : EJHG|October 3, 2002
Testing for BRCA1 mutations: a cost-effectiveness analysisChristine Sevilla, Jean-Paul Moatti, Claire Julian-Reynier, et al.
European Journal of Human Genetics : EJHG|October 3, 2002
Clinical and biochemical characteristics and genotype-phenotype correlation in Finnish variegate porphyria patientsMikael von und zu Fraunberg, Kaisa Timonen, Pertti Mustajoki, et al.
European Journal of Human Genetics : EJHG|June 26, 2003
Identification of 11 novel and common single nucleotide polymorphisms in the interleukin-7 receptor-alpha gene and their associations with multiple sclerosisSuzy M Teutsch, David R Booth, Bruce H Bennetts, et al.
European Journal of Human Genetics : EJHG|June 26, 2003
Muscle glycogenosis with low phosphorylase kinase activity: mutations in PHKA1, PHKG1 or six other candidate genes explain only a minority of casesBarbara Burwinkel, Bin Hu, Anja Schroers, et al.
European Journal of Human Genetics : EJHG|May 30, 2001
Genetic analysis in Finnish families with inflammatory bowel disease supports linkage to chromosome 3p21P Paavola, T Heliö, M Kiuru, et al.
European Journal of Human Genetics : EJHG|May 30, 2001
Genetic polymorphism of MUC7: allele frequencies and association with asthmaH J Kirkbride, J G Bolscher, K Nazmi, et al.
European Journal of Human Genetics : EJHG|May 30, 2001
High-resolution physical and transcript map of human chromosome 2p21 containing the sitosterolaemia locusK Lu, M H Lee, J D Carpten, et al.
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