Search Results - Rosby, O

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  1. 1
    CAPN3 mutation c. 643-663del21 identified in 52 Norwegian patients belonging to 24 families is associated with dominant calpainopathy

    CAPN3 mutation c. 643-663del21 identified in 52 Norwegian patients belonging to 24 families is associated with dominant calpainopathy by Van Ghelue, M, Wahl, C, Arntzen, K, Loseth, S, Bindoff, L, Sveberg, L, Rosby, O, Popperud, T, Rasmussen, M, Halvorsen, H, Lindal, S, Jonsrud, C, Orstavik, K

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  2. 2
    LPA gene: interaction between the apolipoprotein(a) size (‘kringle IV’ repeat) polymorphism and a pentanucleotide repeat polymorphism influences Lp(a) lipoprotein level

    LPA gene: interaction between the apolipoprotein(a) size (‘kringle IV’ repeat) polymorphism and a pentanucleotide repeat polymorphism influences Lp(a) lipoprotein level by Røsby, O., Berg, K.

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  3. 3
    Sequence conservation in kringle IV-type 2 repeats of the LPA gene

    Sequence conservation in kringle IV-type 2 repeats of the LPA gene by Røsby, Oddveig, Aleström, Peter, Berg, Kåre

    Published in Atherosclerosis
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  4. 4
    G.P.160 - CAPN3 mutation c. 643-663del21 identified in 52 Norwegian patients belonging to 24 families is associated with dominant calpainopathy

    G.P.160 - CAPN3 mutation c. 643-663del21 identified in 52 Norwegian patients belonging to 24 families is associated with dominant calpainopathy by Van Ghelue, M., Wahl, C., Arntzen, K., Loseth, S., Bindoff, L., Sveberg, L., Rosby, O., Popperud, T., Rasmussen, M., Halvorsen, H., Lindal, S., Jonsrud, C., Orstavik, K.

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  5. 5
    High-degree sequence conservation in LPA kringle IV-type 2 exons and introns

    High-degree sequence conservation in LPA kringle IV-type 2 exons and introns by Rösby, Oddveig, Aleström, Peter, Berg, Kåre

    Published in Clinical genetics
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  6. 6
    Screening for point mutations in exon 10 of the low density lipoprotein receptor gene by analysis of single-strand conformation polymorphisms : detection of a nonsense mutation-FH469→Stop

    Screening for point mutations in exon 10 of the low density lipoprotein receptor gene by analysis of single-strand conformation polymorphisms : detection of a nonsense mutation-FH4... by LEREN, T. P, SOLBERG, K, RØDNINGEN, O. K, RØSBY, O, TONSTAD, S, OSE, L, BERG, K

    Published in Human genetics
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