1、

HHT is an autosomal dominant disordercharacterized by vascular dysplasia.

HHT是常染色体显性遗传性血管发育异常的一种疾病.

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2、

Objective : To study the relationship between autosomal polymorphism and male infertility.

目的: 探讨常染色体多态性对男性不育的影响.

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3、

Familial Adenomatous Polyposis Syndrome ( FAP ) is an autosomal dominant hereditary condition.

家族性结直肠瘜肉综合症 ( FAP ) 是一种显性的常染色体遗传病.

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4、

As with familial adenomatous polyposis, the inheritance pattern is autosomal dominant.

家族性腺瘤息肉病的遗传方式是常染色体显性遗传.

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5、

Hereditary Non-Polyposis Colorectal Cancer Syndrome ( HNPCC ) is an autosomal dominant hereditary condition.

遗传性( 非 瘜 肉 ) 结直肠癌是一种显性的常染色体遗传病.

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6、

Neurofibromatosis is one of autosomal-dominant neurogenetic diseases with relatively low incidence.

神经纤维瘤病是一常染色体显性遗传性疾病,临床上较为少见.

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7、

Two main modes of inheritance exist: X-linked and autosomal dominant.

本病存在两种主要的遗传方式: X - 连锁型和常染色体显性型.

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8、

Certain autosomal translocations in the heterozygous state can be fully viable.

呈杂合子状态的某些常染色体易位完全可以生活的.

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9、

This disorder is inherited as an autosomal dominant trait.

本病作为常染色体显性传递.

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10、

The genetic analysis showed that this disease was caused by autosomal dominant inheritance.

遗传分析表明,该疾病属常染色体显性遗传.

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11、

This disease for autosomal dominant inheritance, and its development and sun-related.

本病为常染色体显性遗传, 其发展与日晒有关.

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12、

According to genetic analysis, this disease is caused by autosomal dominant inheritance.

经过遗传分析, 认为该畸形属常染色体显性遗传.

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13、

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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14、

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.

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15、

Autosomal means it is passed on and expressed equally in males or females.

正常基因染色体意思是指可以平等地传递给公犬或母犬.

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16、

70 patients ( 63.6%) had positive family history and they showed mostly autosomal dominant inheritance. The rate of consanguinity was 6.9%.

有家族史者70例(63.6%),其中常染色体显性遗传17个家系,近亲结婚者5个家系(6.9%)。

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17、

The results showed that a pat ˉ tern of autosomal dominant inheritance was noticed in all three families.

结果3家系共20例患者,遗传方式均呈常染色体显性遗传;

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18、

Conclusion: The genetics of the true pattern in human palmar hypothenar area may belong to autosomal dominant inheritance.

结论:手掌小鱼际区真实花纹可能属于常染色体显性遗传。

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19、

Conclusions ( 1) HNPCC is of autosomal dominant inheritance ( AD).

结论(1)该家族呈常染色体显性遗传;

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20、

Two sensory defect congenital nystagmus families accompanying with congenital aniridia showed autosomal dominant inheritance.

2个先天性感觉缺陷性眼球震颤家系皆伴有先天性无虹膜,呈常染色体显性遗传。

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