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- 1 Alpha hydroxylase gene knockout mice 1α羟化酶基因敲除小鼠
- 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
- Keywords hydroxylase deficiency Gonadal dysgenesis Chromosome karotype; 羟化酶缺乏;性发育异常;染色体核型;
- 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 researches are concerned with alpha rays. 这些研究是关于阿尔法射线的。
- 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
- I have a slight calcium deficiency. 我有点缺钙。
- 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;
- 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;
- The child has a calcium deficiency. 那孩子缺钙。
- 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
- Wheat is the alpha and omega of their diet. 小麦是他们的主要食物。
- 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
- The researches are concerned with alpha rays . 这些研究都是关于阿尔法射线的。
- 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。
- In physics, this principle is alpha and omega. 这条原理在物理学中极为重要。
- "You get this alpha male effect," Underhill says. 他说，“这样就会出现男性至上的效应。”
- Aleph, alpha: nought, nought, one. 阿列夫，阿尔法，零，零，一。
