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KRAHE, RALF
One or more keywords matched the following items that are connected to
KRAHE, RALF
Item Type
Name
Concept
Finland
Academic Article
Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1.
Academic Article
Multiple founder effects and geographical clustering of BRCA1 and BRCA2 families in Finland.
Academic Article
Involvement of BRCA1 and BRCA2 in breast cancer in a western Finnish sub-population.
Academic Article
Haplotype analysis in Icelandic and Finnish BRCA2 999del5 breast cancer families.
Academic Article
High frequency of co-segregating CLCN1 mutations among myotonic dystrophy type 2 patients from Finland and Germany.
Academic Article
Population frequency of myotonic dystrophy: higher than expected frequency of myotonic dystrophy type 2 (DM2) mutation in Finland.
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Finland