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; Astrom E; Nordgren A; Taylan F; Dahllof G
Article: ORPHANET JOURNAL OF RARE DISEASES. 2018;13(1):145
Dentinogenesis imperfecta type II in Swedish children and adolescents
Andersson K; Malmgren B; Astrom E; Dahllof 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; Dahllof G; Lindahl K; Kindmark A; Grigelioniene G; Astrom 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; Dahllof G; Astrom E

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