X-linked recessive

The inheritance pattern of EDMD includes X-linked recessive, autosomal dominant and recessive modes.

其遗传方式为X - 连锁隐性 、 染色体显性和隐性遗传.

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Genetic analysis showed that the disease is inherited in X-linked recessive heredity. Female carriers have partial symptoms.

遗传学分析表明该病为X连锁隐性遗传，携带者也有不同程度的表现。

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AIS, the X-linked recessive genetic disease, is the mutation of androgen receptor gene in the X chromosome and the defect of androgen receptor of the cell membrane, resulting in androgen insensitivity.

AIS属于X连锁隐性遗传病，是位于X染色体上决定雄激素受体的基因发生突变，引起雄激素靶细胞膜上的雄激素受体缺陷，造成对雄激素不敏感。

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It is universally recognized that the mode of EV transmission may likely be autosomal recessive, but autosomal dominant and X-linked recessive inheritance have also been reported.

通常认为EV是一种常染色体隐性遗传病，但是也有常染色体显性遗传及x连锁隐形遗传等多种遗传方式的报道，揭示了其遗传异质性。

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testicular feminization syndrome, the most common type of male pseudohermaphroditism, is an x-linked recessive disorder.

睾丸女性化综合征是一种X连锁的隐性遗传病，为男性假两性畸形中最常见的类型。

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It is concluded that this is a MSS family X-Linked recessive inheritance.

结论认为该MSS家系为X连锁隐性遗传。

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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.

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EDA is X-linked recessive inheritance, whose clinical symptoms is more severe for the male patients and phenotype is typical.

EDA一般呈X连锁隐性方式遗传，男性表型明显且临床症状严重。

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Conclusion: Mutations of ALD gene is the causes of X-linked recessive adrenoleukodystrophy in Chinese population.

结论ALD基因突变是中国人X-连锁隐性遗传ALD发病原因之一。

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In families, The inheritance patterns are autosomal dominant, autosomal recessive or X-linked recessive.

在家族中，致病基因可以常染色体显性、常染色体隐性或X连锁遗传的方式传递。

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There are three kinds of inherited patterns including autosomal dominant, autosomal recessive and X-linked recessive in inherited congenital cataract.

与遗传有关的先天性白内障有多种遗传方式，其致病基因、基因突变的位点和引起先天性白内障的表现型相继被发现。

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It is compatible with the X-linked recessive inheritance.

该病症符合X-连锁隐性遗传。

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Background: Norrie disease ( ND) is an X-linked recessive disorder characterized by very early childhood blindness due to degenerative and proliferative changes of the neuroretina.

背景：诺里病（Norrie Disease，ND）是一种罕见的由于神经视网膜退行性和增生性改变导致先天或早发性双目失明，呈X染色体连锁隐性遗传。

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Objective To find a way of sampling without any wound and quick diagnosis of fetal sex and its application in X-linked recessive inheritance.

目的建立一种非创伤性的取材和快速胎儿性别诊断方法，并应用于X连锁遗传病的产前诊断。

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Will be received by the nucleated red blood cells used for X-linked recessive genetic diseases ( DMD) in the fetal prenatal diagnosis for non-invasive prenatal genetic diagnosis to provide a reliable basis and experimental methods.

将所获得的有核红细胞用于X连锁隐性遗传病（DMD）的胎儿产前诊断中，为无创伤性产前基因诊断提供可靠的实验依据和方法。

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Methods Genomic DNA was extracted from the peripheral lymphocytes of 10 family members from a X-linked recessive pedigree with dilated cardiomyopathy and 100 healthy controls.

方法从10位X-连锁扩张型心肌病家系成员及100位正常人外周血淋巴细胞中提取基因组DNA。

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