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- BH4 responsive phenylalanine hydroxylase deficiency BH4反應性苯丙氨酸羥化酶缺乏癥
- Protocollagen lysyl hydroxylase deficiency 前膠原賴(lài)氨酸羥化酶缺乏
- phenylalanine hydroxylase deficiency 苯丙氨酸羥化酶缺乏癥, 苯丙酮尿癥, 苯丙氨酸羥化酶缺乏
- Keywords hydroxylase deficiency Gonadal dysgenesis Chromosome karotype; 羥化酶缺乏;性發(fā)育異常;染色體核型;
- Clinical and gene detection of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency 四氫生物蝶呤反應性苯丙氨酸羥化酶缺乏癥的臨床和基因檢測
- Clinical and genetic analysis of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency 四氫生物蝶呤反應性苯丙氨酸羥化酶缺乏癥的臨床與基因研究
- Keywords hydroxylase deficiency;Adrenal hyperplasia;congenital;CYP21;Steroid 21-monooxygenase; 羥化酶缺乏癥;腎上腺增生;先天性;CYP21基因;甾類(lèi)21-單加氧酶;
- Keywords congenital adrenal hyperplasia;21 hydroxylase deficiency;17-hydroxy progesterone; 先天性腎上腺增生;21羥化酶缺陷癥;17羥孕酮;
- Comparison of phenotype and genotype distribution among three types of Chinese patients with 21 - hydroxylase deficiency 不同類(lèi)型21-羥化酶缺乏癥的臨床表型和基因型對比研究
- Screening and diagnosis of tetrahydrobiopterin responsive phenylalanine hydroxylase deficiency with tetrahydrobiopterin loading test 四氫生物蝶呤負荷試驗診斷四氫生物蝶呤反應性苯丙氨酸羥化酶缺乏癥的臨床研究
- I have a slight calcium deficiency. 我有點(diǎn)缺鈣。
- 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. 羥化酶缺乏癥是引起先天性腎上腺增生癥的主要病因之一,由編碼該酶的CYP11B1基因突變引起。
- The child has a calcium deficiency. 那孩子缺鈣。
- 21 hydroxylase deficiency 21羥化酶缺陷癥
- The deficiency of this plan is very clear and it can't possibly succeed. 這項計劃的缺陷是很明顯的，它不可能成功。
- The deficiency in this plan is very clear. 這個(gè)計劃的不足之處顯而易見(jiàn)。
- The result in either case is an energy deficiency. 不論哪種情況結果都會(huì )導致能量損失。
- It is diligence that makes up for deficiency. 勤能補拙。
- The invention also relates to tyrosine hydroxylase revulsant. 本發(fā)明化合物是酪氨酸羥化酶誘導劑。
- The deficiency in this plan be very clear . 這個(gè)計劃的不足之處顯而易見(jiàn)。
