Anna Wedell

Disorders of sex development.

A. Nordenström, A. Wedell, M. Barbaro, 2011, Seminars in fetal & neonatal medicine.

Effects of missense mutations and deletions on membrane anchoring and enzyme function of human steroid 21-hydroxylase (P450c21).

S. Lajic, A. Wedell, M. Holst, 1999, Biochemical and biophysical research communications.

An Update on the Molecular Genetics of Congenital Adrenal Hyperplasia: Diagnostic and Therapeutic Aspects

A. Wedell, Anna Wedell, 1998, Journal of pediatric endocrinology & metabolism : JPEM.

No Mutations in the PSMC3IP Gene Identified in a Swedish Cohort of Women with Primary Ovarian Insufficiency

L. Karlsson, A. Hirschberg, E. Iwarsson, 2014, Sexual Development.

Partial Deletion of the NR5A1 (SF1) Gene Detected by Synthetic Probe MLPA in a Patient with XY Gonadal Disorder of Sex Development

L. Looijenga, M. Cools, A. Wedell, 2011, Sexual Development.