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- Keywords congenital adrenal hyperplasia;21 hydroxylase deficiency;17-hydroxy progesterone; 先天性肾上腺增生;21羟化酶缺陷症;17羟孕酮;
- 21 hydroxylase deficiency 21羟化酶缺陷症
- BH4 responsive phenylalanine hydroxylase deficiency BH4反应性苯丙氨酸羟化酶缺乏症
- Protocollagen lysyl hydroxylase deficiency 前胶原赖氨酸羟化酶缺乏
- phenylalanine hydroxylase deficiency 苯丙氨酸羟化酶缺乏症, 苯丙酮尿症, 苯丙氨酸羟化酶缺乏
- Comparison of phenotype and genotype distribution among three types of Chinese patients with 21 - hydroxylase deficiency 不同类型21-羟化酶缺乏症的临床表型和基因型对比研究
- Keywords hydroxylase deficiency Gonadal dysgenesis Chromosome karotype; 羟化酶缺乏;性发育异常;染色体核型;
- I have a slight calcium deficiency. 我有点缺钙。
- He entered on his inheritance when he was 21. 他21岁时继承了财产。
- Clinical and gene detection of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency 四氢生物蝶呤反应性苯丙氨酸羟化酶缺乏症的临床和基因检测
- The cheque was presented for payment on 21 March. 这张支票是在3月21日兑现的。
- Clinical and genetic analysis of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency 四氢生物蝶呤反应性苯丙氨酸羟化酶缺乏症的临床与基因研究
- A person reaches his majority at the age of 21. 一个人二十一岁达到法定成年。
- Keywords hydroxylase deficiency;Adrenal hyperplasia;congenital;CYP21;Steroid 21-monooxygenase; 羟化酶缺乏症;肾上腺增生;先天性;CYP21基因;甾类21-单加氧酶;
- The child has a calcium deficiency. 那孩子缺钙。
- Screening and diagnosis of tetrahydrobiopterin responsive phenylalanine hydroxylase deficiency with tetrahydrobiopterin loading test 四氢生物蝶呤负荷试验诊断四氢生物蝶呤反应性苯丙氨酸羟化酶缺乏症的临床研究
- hydroxylase deficiency is one of the main causes of congenital adrenal hyperplasia (CAH),which is caused by the mutation of CYP11B1 gene that encodes the enzyme. 羟化酶缺乏症是引起先天性肾上腺增生症的主要病因之一,由编码该酶的CYP11B1基因突变引起。
- A cow's estrus cycle averages 21 days. 母牛的发情周期平均为21天。
- For more on scrollbars, see Chapter 21. 关于滚动条的更多信息参见第21章。
- So what 21) awaits movie fans in the sequel? 那麽，续集中有什麽等著影迷呢?
