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.
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| Description | scientific article |
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author: Kirstine Stochholm Leendert Looijenga Michael Knudsen Søren Vang |
| Publication date | December 2, 2017 |
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