Authors:
Baptista, MJ
Fairbrother, UL
Howard, CM
Farrer, MJ
Davies, GE
Trikka, D
Maratou, K
Redington, A
Greve, G
Njolstad, PR
Kessling, AM
Citation: Mj. Baptista et al., Heterotrisomy, a significant contributing factor to ventricular septal defect associated with Down syndrome?, HUM GENET, 107(5), 2000, pp. 476-482
Authors:
Bjorkhaug, L
Sovik, O
Bell, GI
Njolstad, PR
Molven, A
Citation: L. Bjorkhaug et al., A simple test for the high-frequency P291fsinsC mutation in the HNF1 alpha/MODY3 gene, DIABETOLOG, 43(6), 2000, pp. 818-819
Authors:
Bjorkhaug, L
Ye, HG
Horikawa, Y
Sovik, O
Molven, A
Njolstad, PR
Citation: L. Bjorkhaug et al., MODY associated with two novel hepatocyte nuclear factor-1 alpha loss-of-function mutations (P112L and Q466X), BIOC BIOP R, 279(3), 2000, pp. 792-798
Authors:
Lindner, TH
Njolstad, PR
Horikawa, Y
Bostad, L
Bell, GI
Sovik, O
Citation: Th. Lindner et al., A novel syndrome of diabetes mellitus, renal dysfunction and genital malformation associated with a partial deletion of the pseudo-POU domain of hepatocyte nuclear factor-1 beta, HUM MOL GEN, 8(11), 1999, pp. 2001-2008