Authors:
Pritchard-Jones, K
Rahman, N
Gerrard, M
Variend, D
King-Underwood, L
Citation: K. Pritchard-jones et al., Familial Wilms tumour resulting from WT1 mutation: intronic polymorphism causing artefactual constitutional homozygosity, J MED GENET, 37(5), 2000, pp. 377-379
Authors:
Rahman, N
Abidi, F
Ford, D
Arbour, L
Rapley, E
Tonin, P
Barton, D
Batcup, G
Berry, J
Cotter, F
Davison, V
Gerrard, M
Gray, E
Grundy, R
Hanafy, M
King, D
Lewis, I
Luethy, AR
Madlensky, L
Mann, J
O'Meara, A
Oakhill, T
Skolnick, M
Strong, L
Variend, D
Narod, S
Schwartz, C
Pritchard-Jones, K
Stratton, MR
Citation: N. Rahman et al., Confirmation of FWT1 as a Wilms' tumour susceptibility gene and phenotypiccharacteristics of Wilms' tumour attributable to FWT1, HUM GENET, 103(5), 1998, pp. 547-556