Anne Nørremølle

Anne Nørremølle

Associate Professor


Publication year:
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1 - 4 out of 4Page size: 10
  1. 1993
  2. 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

  3. 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

  4. 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

  5. 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

ID: 3886