go top

羟化酶缺陷

专业释义

  • c11-hydroxylase defect

·2,447,543篇论文数据,部分数据来源于NoteExpress

双语例句

  • 羊水细胞DNA分析先天性肾上腺皮质增生症21-羟化酶缺陷产前诊断可靠方法

    DNA analysis of amniocytes was a feasible method for the prenatal diagnosis of congenital adrenal hyperplasia with 21-hydroxylase deficiency.

    youdao

  • 结论羊水细胞DNA分析先天性肾上腺皮质增生2 1羟化酶缺陷产前诊断可靠方法

    Conclusion DNA analysis of amniocytes was a feasible method for the prenatal diagnosis of congenital adrenal hyperplasia with 21-hydroxylase deficiency.

    youdao

  • 目的分析1921化酶缺陷症(21OHD)患者临床和随访资料提高该病的诊断治疗水平

    Objective Clinical data of 19 Chinese patients with 21 hydroxylase deficiency (21OHD) were analyzed to improve the diagnosis and treatment level.

    youdao

更多双语例句
$firstVoiceSent
- 来自原声例句
小调查
请问您想要如何调整此模块?

感谢您的反馈,我们会尽快进行适当修改!
进来说说原因吧 确定
小调查
请问您想要如何调整此模块?

感谢您的反馈,我们会尽快进行适当修改!
进来说说原因吧 确定