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-Reference-Cited by-同舟云学术

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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

Published:2017 Issue:5-6 Volume:11 Page:262-268
ISSN:1661-5425
Container-title:Sexual Development
language:en
Short-container-title:Sex Dev

Author:

Gravholt Claus H.,Dollerup Ole L.,Duval Lone,Mejlgaard Else,Stribolt Katrine,Vang Søren,Laursen Britt E.,Knudsen Michael,Thorsen Kasper,Hersmus Remko,Looijenga Leendert H.J.,Stochholm Kirstine

Publisher

S. Karger AG

Subject

Developmental Biology,Embryology,Endocrinology, Diabetes and Metabolism

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genomic instability in individuals with sex determination defects and germ cell cancer;Cell Death Discovery;2023-05-23

2. Rare Case of a Turner Syndrome Patient with Metastatic Dysgerminoma and No Y-Chromosomal Material with Pathogenic Variants Found in KIT and MTOR;Sexual Development;2023

3. Cancer occurrence in Turner syndrome and the effect of sex hormone substitution therapy;European Journal of Endocrinology;2021-01

4. Dysgerminoma with a Somatic Exon 17 KIT Mutation and SHH Pathway Activation in a Girl with Turner Syndrome;Diagnostics;2020-12-10

5. Clinical case report;Medicine;2020-03

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