Lars Hansen

Lars Hansen

No job title VIP

  • Det Kgl. Bibliotek - Universitetsbibliotekarens ledelsessekretariat

    Postbox 2149

    1016 København K


Publication year:
  1. 2017
  2. Published

    A novel mutation in CDK5RAP2 gene causes primary microcephaly with speech impairment and sparse eyebrows in a consanguineous Pakistani family

    Abdullah, U., Farooq, M., Mang, Y., Marriam Bakhtiar, S., Fatima, A., Hansen, Lars, Kjaer, K. W., Larsen, Lars Allan, Faryal, S., Tommerup, Niels & Mahmood Baig, S., Dec 2017, In: European Journal of Medical Genetics. 60, 12, p. 627-630 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

ID: 174515075