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Arbour, L
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Abidi, F
Tranchemontagne, J
Ford, D
Narod, S
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Foulkes, WD
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Stratton, MR
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Platt, R
Gilfix, BM
Rosenblatt, DS
Gravel, RA
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Rozen, R
Citation: B. Christensen et al., Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects, AM J MED G, 84(2), 1999, pp. 151-157
Citation: R. Bishai et al., Intrauterine exposure to clomiphene and neonatal persistent hyperplastic primary vitreous, TERATOLOGY, 60(3), 1999, pp. 143-145
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Shkolny, DL
Beitel, LK
Ginsberg, J
Pekeles, G
Arbour, L
Pinsky, L
Trifiro, MA
Citation: Dl. Shkolny et al., Discordant measures of androgen-binding kinetics in two mutant androgen receptors causing mild or partial androgen insensitivity, respectively, J CLIN END, 84(2), 1999, pp. 805-810
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