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Results 1 - 6 of 6 for Norwegian
  1. HMBS gene 
    ... O, Sandberg S, Apold J. Haplotype analysis of Norwegian and Swedish patients with acute intermittent porphyria (AIP): ...
    https://medlineplus.gov/genetics/gene/hmbs - Genetics
  2. ACTG1 gene 
    ... mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not ...
    https://medlineplus.gov/genetics/gene/actg1 - Genetics
  3. Breast cancer 
    ... or eastern European) Jewish heritage and people of Norwegian, Icelandic, or Dutch ancestry. Cancers occur when a ...
    https://medlineplus.gov/genetics/condition/breast-cancer - Genetics
  4. ABCC8 gene 
    ... Molven A. The spectrum of ABCC8 mutations in Norwegian patients with congenital hyperinsulinism of infancy. Clin Genet. ...
    https://medlineplus.gov/genetics/gene/abcc8 - Genetics
  5. Congenital hyperinsulinism 
    ... Molven A. The spectrum of ABCC8 mutations in Norwegian patients with congenital hyperinsulinism of infancy. Clin Genet. ...
    https://medlineplus.gov/.../condition/congenital-hyperinsulinism - Genetics
  6. INS gene 
    ... Aarskog D, Undlien DE, Joner G, Sovik O; Norwegian Childhood Diabetes Study Group; Bell GI, Njolstad PR. ...
    https://medlineplus.gov/genetics/gene/ins - Genetics