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Results: 1-5 |
Results: 5

Authors: Njolstad, PR Sovik, O Cuesta-Munoz, A Bjorkhaug, L Massa, O Barbetti, F Undlien, DE Shiota, C Magnuson, MA Molven, A Matschinsky, FM Bell, GI
Citation: Pr. Njolstad et al., Neonatal diabetes mellitus due to complete glucokinase deficiency., N ENG J MED, 344(21), 2001, pp. 1588-1592

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
Risultati: 1-5 |