A Rare Case of Embryonal Carcinoma in a Patient with Turner Syndrome without Y Chromosomal Material but Mutations in KIT, AKT1, and ZNF358 Demonstrated Using Exome Sequencing

CH Gravholt, OL Dollerup, L Duval, E Mejlgaard, K Stribolt, S Vang, BE Laursen, M Knudsen, K Thorsen, Remko Hersmus, LHJ (Leendert) Looijenga, K Stochholm

Research output: Contribution to journalArticleAcademicpeer-review

5 Citations (Scopus)
Original languageUndefined/Unknown
Pages (from-to)262-268
Number of pages7
JournalSexual Development
Issue number5-6
Publication statusPublished - 2017

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