Genetic variation in ICF syndrome: Evidence for genetic heterogeneity
Wijmenga, Cisca, Hansen, R. Scott, Gimelli, Giorgio, Björck, Erik J., Davies, E. Graham, Valentine, David, Belohradsky, Bernd H., van Dongen, Jacques J., Smeets, Dominique F.C.M., van den Heuvel, Lambert P.W.J., Luyten, Jan A.F.M., Strengman, Eric, Weemaes, Corry, Pearson, Peter L.
Published in Human mutation (01.12.2000)
Published in Human mutation (01.12.2000)
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Journal Article
Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in Scandinavia
Jonasson, J, Juvonen, V, Sistonen, P, Ignatius, J, Johansson, D, Björck, E J, Wahlström, J, Melberg, A, Holmgren, G, Forsgren, L, Holmberg, M
Published in European journal of human genetics : EJHG (2000)
Published in European journal of human genetics : EJHG (2000)
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Journal Article
Early prenatal diagnosis of the ICF syndrome
Björck, Erik J., Bui, The-Hung, Wijmenga, Cisca, Grandell, Ulla, Nordenskjöld, Magnus
Published in Prenatal diagnosis (01.10.2000)
Published in Prenatal diagnosis (01.10.2000)
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Journal Article