Anne Nørremølle

Anne Nørremølle

Associate Professor


Publication year:
All
1 - 4 out of 4Page size: 10
  1. 1992
  2. Published

    Exclusion of DNA changes in the *GB-subunit of the C-GMP phosphodiesterase gene as the cause for Huntington's disease

    Riess, O., Nørremølle, Anne, Collins, C., Mah, D., Weber, B. & Hayden, M. R., 1992, In: Nature Genetics. 1, p. 104-108

    Research output: Contribution to journal › Journal article › Research › peer-review

  3. Published

    Linkage studies and mutation analysis of the PDEB gene in 23 families with Leber congenital amaurosis

    Riess, O., Weber, B., Nørremølle, Anne, Shaikh, R. A., Hayden, M. R. & Musarella, M. A., 1992, In: Human Mutation. 1, 6, p. 478-85 7 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  4. Published

    Nucleotide sequence and PCR-amplification of a polymorphic MboI site in human DNA marker D4S95 linked to the Huntington disease locus.

    Nørremølle, Anne, Sørensen, S. A. & Arctander, P., 1992, In: Clinical Genetics. 42, p. 210-211 2 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  5. Published

    The search for mutations in the gene for the beta subunit of the cGMP phosphodiesterase (PDEB) in patients with autosomal recessive retinitis pigmentosa

    Riess, O., Nørremølle, Anne, Weber, B., Musarella, M. A. & Hayden, M. R., 1992, In: American Journal of Human Genetics. 51, 4, p. 755-62 7 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

ID: 3886