Authors:
Bignell, GR
Warren, W
Seal, S
Takahashi, M
Rapley, E
Barfoot, R
Green, H
Brown, C
Biggs, PJ
Lakhani, SR
Jones, C
Hansen, J
Blair, E
Hofmann, B
Siebert, R
Turner, G
Evans, DG
Schrander-Stumpel, C
Beemer, FA
van den Ouweland, A
Halley, D
Delpech, B
Cleveland, MG
Leigh, I
Leisti, J
Rasmussen, S
Wallace, MR
Fenske, C
Banerjee, P
Oiso, N
Chaggar, R
Merrett, S
Leonard, N
Huber, M
Hohl, D
Chapman, P
Burn, J
Swift, S
Smith, A
Ashworth, A
Stratton, MR
Citation: Gr. Bignell et al., Identification of the familial cylindromatosis tumour-suppressor gene, NAT GENET, 25(2), 2000, pp. 160-165
Authors:
Takahashi, M
Rapley, E
Biggs, PJ
Lakhani, SR
Cooke, D
Hansen, J
Blair, E
Hofmann, B
Siebert, R
Turner, G
Evans, DG
Schrander-Stumpel, C
Beemer, FA
van Vloten, WA
Breuning, MH
van den Ouweland, A
Halley, D
Delpech, B
Cleveland, M
Leigh, I
Chapman, P
Burn, J
Hohl, D
Gorog, JP
Seal, S
Mangion, J
Warren, W
Bignell, G
Stratton, MR
Citation: M. Takahashi et al., Linkage and LOH studies in 19 cylindromatosis families show no evidence ofgenetic heterogeneity and refine the CYLD locus on chromosome 16q12-q13, HUM GENET, 106(1), 2000, pp. 58-65
Authors:
van Slegtenhorst, M
Verhoef, S
Tempelaars, A
Bakker, L
Wang, Q
Wessels, M
Bakker, R
Nellist, M
Lindhout, D
Halley, D
van den Ouweland, A
Citation: M. Van Slegtenhorst et al., Mutational spectrum of the TSC1 gene in a cohort of 225 tuberous sclerosiscomplex patients: no evidence for genotype-phenotype correlation, J MED GENET, 36(4), 1999, pp. 285-289