Human Mutation, 1059-7794

Journal

Publications

  1. 2007
  2. Published

    Genotype-phenotype correlations in von Hippel-Lindau disease

    Emma Woodward & Eamonn Maher, 1 Feb 2007, In : Human Mutation. 28, 2, p. 143-149 7 p.

    Research output: Contribution to journalArticle

  3. 2005
  4. Published
  5. Published

    Thirteen novel mutations in the NR0B1 (DAX1) gene as cause of adrenal hypoplasia congenita

    Nils Krone, 2005, In : Human Mutation. 25, 5, p. 502-3 2 p.

    Research output: Contribution to journalArticlepeer-review

  6. 2003
  7. Published
  8. 2001
  9. Published

    WFS1/wolframin mutations, Wolfram syndrome, and associated diseases

    Farhat Khanim, Farida Latif & Timothy Barrett, 1 May 2001, In : Human Mutation. 17, 5, p. 357-367 11 p.

    Research output: Contribution to journalArticle

Previous 1 2 3 Next