Kristofer Andersson

Artiklar

Article: ORPHANET JOURNAL OF RARE DISEASES. 2020;15(1):80

Mutations in COL1A1/A2 and CREB3L1 are associated with oligodontia in osteogenesis imperfecta.

Andersson K; Malmgren B; Åström E; Nordgren A; Taylan F; Dahllöf G
Article: ORPHANET JOURNAL OF RARE DISEASES. 2018;13(1):145

Dentinogenesis imperfecta type II in Swedish children and adolescents.

Andersson K; Malmgren B; Åström E; Dahllöf G
Article: PLOS ONE. 2017;12(5):e0176466

Mutations in COL1A1 and COL1A2 and dental aberrations in children and adolescents with osteogenesis imperfecta - A retrospective cohort study.

Andersson K; Dahllöf G; Lindahl K; Kindmark A; Grigelioniene G; Åström E; Malmgren B
Article: ORAL DISEASES. 2017;23(1):42-49

Tooth agenesis in osteogenesis imperfecta related to mutations in the collagen type I genes.

Malmgren B; Andersson K; Lindahl K; Kindmark A; Grigelioniene G; Zachariadis V; Dahllöf G; Åström E

Medicine Doktorsexamen, Institutionen för odontologi, Karolinska Institutet, 2018
Tandläkarexamen, Karolinska Institutet, 2009