Niels Tommerup

Søgeresultater

• 2002

  Gorlin syndrome in a patient with deletion of the distal part of chromosome 9q and fine mapping of the break points with fluorescence in situ hybridization

  Boonen, S. E., Tümer, Z., Tommerup, N., Stahl, D., Rosenberg, T., Kreiborg, S. & Brøndum-Nielsen, K., 2002, Ikke angivet. European Human Genetics Conference 2002, Strasbourg, s. 201-201

  Publikation: Bidrag til bog/antologi/rapport › Konferenceabstrakt i proceedings › Forskning