Matre G - Search Results

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Complete mutation screening and haplotype characterization of the BRCA1 gene in 61 familial breast cancer patients from Norway.

Frost P, Jugessur A, Apold J, Heimdal K, Aloysius T, Eliassen AK, Fauske L, Matre G, Eiken HG. Frost P, et al. Among authors: matre g. Dis Markers. 2005;21(1):29-36. doi: 10.1155/2005/542928. Dis Markers. 2005. PMID: 15735322 Free PMC article.

Polymorphisms in CYP2D6 duplication-negative individuals with the ultrarapid metabolizer phenotype: a role for the CYP2D6*35 allele in ultrarapid metabolism?

Løvlie R, Daly AK, Matre GE, Molven A, Steen VM. Løvlie R, et al. Among authors: matre ge. Pharmacogenetics. 2001 Feb;11(1):45-55. doi: 10.1097/00008571-200102000-00006. Pharmacogenetics. 2001. PMID: 11207030

Familial hyperinsulinemic hypoglycemia caused by a defect in the SCHAD enzyme of mitochondrial fatty acid oxidation.

Molven A, Matre GE, Duran M, Wanders RJ, Rishaug U, Njølstad PR, Jellum E, Søvik O. Molven A, et al. Among authors: matre ge. Diabetes. 2004 Jan;53(1):221-7. doi: 10.2337/diabetes.53.1.221. Diabetes. 2004. PMID: 14693719

Hunting for a hypoglycemia gene: severe neonatal hypoglycemia in a consanguineous family.

Molven A, Rishaug U, Matre GE, Njølstad PR, Søvik O. Molven A, et al. Among authors: matre ge. Am J Med Genet. 2002 Nov 15;113(1):40-6. doi: 10.1002/ajmg.10575. Am J Med Genet. 2002. PMID: 12400064

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