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- It is a common occurrence in dogs and is thought to be a sex-limited autosomal recessive trait. 该疾病常发于犬，并被认为具有限性常染色体隐性遗传特征。
- Oculocutaneous albinism results from an autosomal recessive trait; ocular albinism results from an X-linked recessive trait that causes hypopigmentation only in the iris and the ocular fundus. 结果从眼白化病常染色体隐性性状;眼部白化结果从X连锁隐性性状,只有在虹膜色素缺失原因及眼底。
- a disorder of lipid metabolism that is inherited as an autosomal recessive trait 油脂新陈代谢混乱的一种遗传病症
- a disorder of lipid metabolism that is inherited as an autosomal recessive trait. 油脂新陈代谢混乱的一种遗传病症。
- autosomal recessive trait 常染色体隐性遗传特性
- An organism having a recessive trait. 具隐性性状有机体
- It is usually inherited as an autosomal dominant trait, although autosomal recessive and X-linked inheritance are seen less commonly. 人群中，大部分遗传性白内障是外显率较高的常染色体显性遗传，但也有X连锁和常染色体隐性遗传存在。
- Xeroderma pigmentosum is an autosomal recessive disease. 着色性干皮病是一种常染色体的退行性疾病。
- Colour blindness is a sex-linked recessive trait 20 times more common in men than in women. 色盲是伴性隐性遗传疾病，男性发病率为女性的二十倍。
- Multiple carboxylase deficiency (MCD) is an autosomal recessive disorder of inherited metabolic diseases. 多种羧化酶缺陷症(MCD)是一种常染色体隐性遗传的先天遗传代谢性疾病。
- Harlequin ichthyosis （HI）is a severe subtype of autosomal recessive congenital ichthyoses (ARCI). 丑角样鱼鳞病是常染色体隐性遗传性鱼鳞病的一种严重亚型。
- Results The genetic pattern of IEP is not polygenic but is mainly influenced by autosomal recessive disorders. 结果IEP不符合多基因遗传，而主要为常染色体隐体遗传。
- Congenital adrenal hyperplasia is a genetic disorder transmitted by autosomal recessive pattern. 摘要先天性肾上腺增生症是一种自体隐性遗传病。
- If magic is a recessive trait, then marrying and having children with a Muggle will certainly impair the chances of your family staying magical for the next generation. 如果魔法天赋具有隐性特征，那么与一个麻瓜结合生孩子自然便降低了你家庭的下一代保持魔法天赋的机会。
- It can be autosomal dominant, autosomal recessive, or X-linked mode of inheritance. 他可以是体染色体显性、体染色体隐性、或是性联遗传等方式的遗传疾病。
- The recurrence risk for this disease is, of course, 25% because of the autosomal recessive inheritance pattern. 因为它是常染色体隐性遗传的，所以它在家族中的发病率是25%25。
- We report an infant delivered at 31 weeks gestation with restrictive dermopathy, which is a rare autosomal recessive genodermatosis. 摘要我们报告一拘束性皮肤病变的31周出生婴儿，其为一罕见的，体隐性遗传皮肤病。
- Maple syrup urine disease (MSUD), or branched-chain ketoaciduria, is an autosomal recessive disorder of branched-chain amino acid metabolism. 摘要枫糖尿症是支链氨基酸代谢异常的体染色体隐性遗传疾病。
- The frequencies of non Mongolia wrinkle were 15.41% and 5.42%,the frequencies of autosomal recessive inheritance were 0.3925 and 0.2328 respectively. 蒙古褶为无的出现率分别为15.;41%25和5
- It was also showed that the gene of tolerance to sprouting in RSP derived from Ae. tauschii was inherited as a recessive trait which was controlled by one gene, located on chromosome 2D. 利用RSP对节节麦的抗穗发芽基因进行定位分析，结果表明，RSP的抗穗发芽基因是隐性单基因位于2D染色体上。
