Hakan Cangul

Publications

  1. 2018
  2. Published

    Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism

    18 Oct 2018, In: JCI Insight. 3, 20, 11 p., e99631.

    Research output: Contribution to journalAbstractpeer-review

  3. 2015
  4. Published
  5. 2012
  6. Published
  7. Published
  8. 2010
  9. Published
  10. Published

    Puberty, stress, and sudden death

    Hakan Cangul, 30 Oct 2010, In: Lancet. 376, 9751, p. 1512 1 p.

    Research output: Contribution to journalArticle

  11. Published
  12. Published