英语词汇21-hydroxylase deficiency怎么读，是什么意思，单词翻译、读音、固定搭配用法和短语词组及例句-英汉双解词典

单词

21-hydroxylase deficiency

释义

21-hydroxylase deficiency

翻译

21-hydroxylase不足

以上为机器翻译结果，快速获取精准的人工翻译结果，建议选择有道人工翻译

网络释义

1
?羟化酶缺乏型
...性肾上腺皮质增生症，21羟化酶缺乏型，终身高 [gap=697]Key Words]?congenital adrenal hyperplasia,21-hydroxylase deficiency, final height ...

短语

1
steroid 21-hydroxylase deficiency
羟化酶缺乏
2
mild steroid 21-hydroxylase deficiency
轻度类固醇21
3
severe steroid 21-hydroxylase deficiency
重度类固醇21

双语例句

1
DNA analysis of amniocytes was a feasible method for the prenatal diagnosis of congenital adrenal hyperplasia with 21-hydroxylase deficiency.
羊水细胞DNA分析是先天性肾上腺皮质增生症21-羟化酶缺陷的产前诊断的可靠方法。
2
Conclusion DNA analysis of amniocytes was a feasible method for the prenatal diagnosis of congenital adrenal hyperplasia with 21-hydroxylase deficiency.
结论羊水细胞DNA分析是先天性肾上腺皮质增生症2 1羟化酶缺陷的产前诊断的可靠方法。
3
Objective Clinical data of 19 Chinese patients with 21 hydroxylase deficiency (21OHD) were analyzed to improve the diagnosis and treatment level.
目的分析19例21羟化酶缺陷症（21OHD）患者的临床和随访资料，提高该病的诊断和治疗水平。

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英汉双解词典包含3185865条英汉词条，基本涵盖了全部常用单词的翻译及用法，是英语学习的有利工具。

单词	21-hydroxylase deficiency
释义	21-hydroxylase deficiency 翻译 21-hydroxylase不足以上为机器翻译结果，快速获取精准的人工翻译结果，建议选择有道人工翻译网络释义 1 ?羟化酶缺乏型 ...性肾上腺皮质增生症，21羟化酶缺乏型，终身高 [gap=697]Key Words]?congenital adrenal hyperplasia,21-hydroxylase deficiency, final height ... 短语 1 steroid 21-hydroxylase deficiency 羟化酶缺乏 2 mild steroid 21-hydroxylase deficiency 轻度类固醇21 3 severe steroid 21-hydroxylase deficiency 重度类固醇21 双语例句 1 DNA analysis of amniocytes was a feasible method for the prenatal diagnosis of congenital adrenal hyperplasia with 21-hydroxylase deficiency. 羊水细胞DNA分析是先天性肾上腺皮质增生症21-羟化酶缺陷的产前诊断的可靠方法。 2 Conclusion DNA analysis of amniocytes was a feasible method for the prenatal diagnosis of congenital adrenal hyperplasia with 21-hydroxylase deficiency. 结论羊水细胞DNA分析是先天性肾上腺皮质增生症2 1羟化酶缺陷的产前诊断的可靠方法。 3 Objective Clinical data of 19 Chinese patients with 21 hydroxylase deficiency (21OHD) were analyzed to improve the diagnosis and treatment level. 目的分析19例21羟化酶缺陷症（21OHD）患者的临床和随访资料，提高该病的诊断和治疗水平。
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