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Results: 1-4 |
Results: 4

Authors: Wijmenga, C Hansen, RS Gimelli, G Bjorck, EJ Davies, EG Valentine, D Belohradsky, BH van Dongen, JJ Smeets, DFCM van den Heuvel, LPWJ Luyten, JAFM Strengman, E Weemaes, C Pearson, PL
Citation: C. Wijmenga et al., Genetic variation in ICF syndrome: Evidence for genetic heterogeneity, HUM MUTAT, 16(6), 2000, pp. 509-517

Authors: Jonasson, J Juvonen, V Sistonen, P Ignatius, J Johansson, D Bjorck, EJ Wahlstrom, J Melberg, A Holmgren, G Forsgren, L Holmberg, M
Citation: J. Jonasson et al., Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in Scandinavia, EUR J HUM G, 8(12), 2000, pp. 918-922

Authors: Bjorck, EJ Bui, TH Wijmenga, C Grandell, U Nordenskjold, M
Citation: Ej. Bjorck et al., Early prenatal diagnosis of the ICF syndrome, PRENAT DIAG, 20(10), 2000, pp. 828-831

Authors: Bjorck, EJ Anderlid, BM Blennow, E
Citation: Ej. Bjorck et al., Maternal isodisomy of chromosome 9 with no impact on the phenotype in a woman with two isochromosomes: i(9p) and i(9q), AM J MED G, 87(1), 1999, pp. 49-52
Risultati: 1-4 |