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Whole genome sequencing identifies a cryptic SOX9 regulatory element duplication underlying a case of 46, XX ovotesticular difference of sexual development

机译：全基因组测序识别隐蔽的SOx9监管元素重复，案例为46，XX ofotorational的性发育差异

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Zhiyu Qian; Katheryn Grand; Andrew Freedman; Maria C. Nieto; Andrea Behlmann; Bahareh M. Schweiger; Pedro A. Sanchez‐Lara;
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1. Duplication of SOX9 is not a common cause of 46,XX testicular or 46,XX ovotesticular DSD [J] . TemelS.G., CangulH. Journal of pediatric endocrinology & metabolism: JPEM . 2013,第1a2期

机译：SOX9的重复不是导致46，XX睾丸或46，XX卵睾DSD的常见原因
2. A Duplication Upstream of SOX9 Associated with SRY Negative 46,XX Ovotesticular Disorder of Sex Development: A Case Report [J] . Eda Mengen, Gülsüm Kayhan, P?nar Kocaay, Journal of Clinical Research in Pediatric Endocrinology . 2020,第3期

机译：<斜体> SOX9 与<斜视> sry 负相关的复制，xx ofotoraticuards性交疾病：案例报告
3. Duplication of SOX9 associated with 46, XX ovotesticular disorder of sex development [J] . Lopez-Hernandez Berenice, Pablo Mendez Juan, Mauricio Coral-Vazquez Ramon, Reproductive biomedicine online . 2018,第1期

机译：复制SOX9与46相关的SOX9，XX ofotteational的性行为疾病
4. A Pipeline for Identifying Integration Sites of Mobile Elements in the Genome Using Next-Generation Sequencing [C] . Raunaq Malhotra, Daniel Elleder, Le Bao, International Conference on Bioinformatics and Computational Biology . 2016

机译：使用下一代测序识别基因组中移动元素集成站点的管道
5. Identifying The Regulatory Role Of Transposable Elements In Mammalian Genomes. [D] . Sundaram, Vasavi. 2016

机译：确定转座因子在哺乳动物基因组中的调控作用。
6. The 46 XX Ovotesticular Disorder of Sex Development With Xq27.1q27.2 Duplication Involving the SOX3 Gene: A Rare Case Report and Literature Review [O] . Jianlong Zhuang, Chunnuan Chen, Jia Li, 2021

机译：46XX ofotteational的性发展疾病与XQ27.1Q27.2涉及SOX3基因的重复：罕见的报告和文献综述
7. The 46, XX Ovotesticular Disorder of Sex Development With Xq27.1q27.2 Duplication Involving the SOX3 Gene: A Rare Case Report and Literature Review [O] . Jianlong Zhuang, Chunnuan Chen, Jia Li, 2021

机译：46，XX ofotteational的性发展疾病与XQ27.1Q27.2涉及SOX3基因的重复：罕见的报告和文献综述

Whole genome sequencing identifies a cryptic SOX9 regulatory element duplication underlying a case of 46, XX ovotesticular difference of sexual development

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