Anne Nørremølle

Anne Nørremølle

Associate Professor


Publication year:
All
51 - 59 out of 59Page size: 10
  1. 1995
  2. Published

    Elongated CAG repeats of the B37 gene in a Danish family with dentatorubro-pallido-luysian atrophy

    Nørremølle, Anne, Nielsen, J. E., Sørensen, S. A. & Hasholt, Lis Frydenreich, 1995, In: Human Genetics. 95, p. 313-318

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

  3. 1993
  4. Published

    DNA analysis of distinct populations suggests multiple origins for the mutation causing Huntington's disease

    Andrew, S., Theilmann, J., Almquist, E., Nørremølle, Anne, Lucotte, G., Anvret, M., Sørensen, S. A., Turpin, J. C. & Hayden, M. R., 1993, In: Clinical Genetics. 43, p. 286-294

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

  5. Published

    Improved PCR conditions for the stretch of (CAG)n repeats causing Huntington's disease

    Riess, O., Nørremølle, Anne, Sørensen, S. A. & Epplen, J. T., 1993, In: Human Molecular Genetics. 2, 6, p. 637

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

  6. Published

    Mapping of the human NMDA receptor subunit (NMDAR1) and the proposed NMDA receptor glutamate-binding subunit (NMDARA1) to chromosomes 9q34.3 and chromosome 8, respectively

    Collins, C., Duff, C., Duncan, A. M., Planells-Cases, R., Sun, W., Nørremølle, Anne, Michaelis, E., Montal, M., Worton, R. & Hayden, M. R., 1993, In: Genomics. 17, 1, p. 237-9 2 p.

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

  7. Published

    Trinucleotide repeat elongation in the Huntington gene in Huntington Disease patients from 71 Danish families

    Nørremølle, Anne, Riess, O., Epplen, J. T., Fenger, K., Hasholt, L. & Sørensen, S. A., 1993, In: Human Molecular Genetics. 2, p. 1475-1476

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

  8. 1992
  9. 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

  10. 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

  11. 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

  12. 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

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