A. Norling

From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disability

P. Georgii‐Hemming, A. Nordgren, J. Eisfeldt, 2019, Genome Medicine.

CBX2 gene analysis in patients with 46,XY and 46,XX gonadal disorders of sex development.

A. Hirschberg, E. Iwarsson, A. Wedell, 2013, Fertility and sterility.

Identification of a duplication within the GDF9 gene and novel candidate genes for primary ovarian insufficiency (POI) by a customized high-resolution array comparative genomic hybridization platform

A. Hirschberg, E. Iwarsson, K. Rodriguez-Wallberg, 2014, Human reproduction.

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.

No Mutations in the PSMC 3 IP Gene Identified in a Swedish Cohort of Women with Primary Ovarian Insufficiency

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

Novel candidate genes for 46,XY gonadal dysgenesis identified by a customized 1 M array-CGH platform.

B. Persson, E. Iwarsson, A. Wedell, 2013, European journal of medical genetics.

Molecular mechanisms in disorders of gonadal development

A. Norling, 2013 .