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
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