Edvard Nordenskjöld

A novel stop mutation in the EDNRB gene in a family with Hirschsprung's disease associated with multiple sclerosis.

D. Nilsson, A. Nordenskjöld, E. Markljung, 2014, Journal of pediatric surgery.

Familial hemophagocytic lymphohistiocytosis type 3 (FHL3) caused by deep intronic mutation and inversion in UNC13D.

H. Ljunggren, B. Fadeel, T. Salmi, 2011, Blood.

Mutation Screening and Array Comparative Genomic Hybridization Using a 180K Oligonucleotide Array in VACTERL Association

A. Nordgren, G. Annéren, E. Sahlin, 2014, PloS one.

Groundwater occurrence and quality in Bulawayo province, Zimbabwe

A. Nygren, Erik Östblom, Edvard Nordenskjöld, 2016 .