Disorders of sex development: insights from targeted gene sequencing of a large international patient cohortStefanie Eggers, Richard King, Ingrid Knarston et al.|Genome biology|2016Cited by 404
Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrumAnne Thorwarth, Heiko Krude, Sarah Schnittert-Hübener et al.|Journal of Medical Genetics|2014Cited by 114
Additional file 2: Figure S1. of Disorders of sex development: insights from targeted gene sequencing of a large international patient cohortStefanie Eggers, Richard King, Simon Sadedin et al.|INDIGO (University of Illinois at Chicago)|2016Cited by 0
Additional file 1: Table S1. of Disorders of sex development: insights from targeted gene sequencing of a large international patient cohortStefanie Eggers, Richard King, Simon Sadedin et al.|University of Groningen research database (University of Groningen / Centre for Information Technology)|2016Cited by 0