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Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|February 28, 1994
[Indirect genetic diagnosis of cystic fibrosis]H Boman, H G Eiken, G FlugeTidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|October 30, 1993
[DNA diagnosis of fragile X syndrome in a family. A new type of heredity--dynamic mutations]H G Eiken, H Boman, J ApoldGene|January 1, 1988
Molecular cloning and characterization of homeo-box-containing genes from Atlantic salmonA Fjose, A Molven, H G EikenTidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|June 11, 1998
[Molecular genetic diagnostics. Technology for detecting mutations in DNA]H G Eiken, A L Børresen-DaleHuman Genetics|August 1, 1996
The Ca(2+)-sensing receptor gene (PCAR1) mutation T151M in isolated autosomal dominant hypoparathyroidismR Løvlie, H G Eiken, J I Sørheim, et al.Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|October 30, 1993
[Analysis of the Duchenne muscular dystrophy gene with PCR analysis in paraffin-embedded tissue. A new diagnostic possibility]J Apold, H G Eiken, L F Engebretsen, et al.FEBS Letters|September 3, 1999
Diverse PAH transcripts in lymphocytes of PKU patients with putative nonsense (G272X, Y356X) and missense (P281L, R408Q) mutationsS Ellingsen, P M Knappskog, J Apold, et al.Gene|December 15, 1988
Structure and neural expression of a zebrafish homeobox sequenceP R Njølstad, A Molven, H G Eiken, et al.Human Mutation|January 1, 1996
PKU mutation G46S is associated with increased aggregation and degradation of the phenylalanine hydroxylase enzymeH G Eiken, P M Knappskog, J Apold, et al.Biochemical and Biophysical Research Communications|December 31, 1987
A zebrafish homeobox-containing gene with embryonic transcriptionH G Eiken, P R Njølstad, A Molven, et al.Pageof 4