autosomal dominant inheritance

[ˌɔ:təuˈsəuməl ˈdɔminənt ɪnˈherɪtəns]
  • 释义

    常染色体显性遗传;

数据更新时间:2025-11-14 01:48:03
1、

The genetic analysis shows it is autosomal dominant inheritance.

遗传学分析结果显示该家系的遗传方式符合常染色体显性遗传规律。

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2、

The transmission accords with autosomal dominant inheritance.

符合常染色体显性遗传。

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3、

Approximately 2/ 3 of the patients have the family history, and follow the autosomal dominant inheritance pattern.

约2/3的患者有家族病史,表现为常染色体显性遗传,余1/3患者为散发病例。

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4、

Result: It's autosomal dominant inheritance in this family.

结果:该家族为常染色体显性遗传家系。

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5、

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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6、

The results indicate that psoriasis is of autosomal dominant inheritance and incomplete phenotype.

认为银屑病属于常染色体显性遗传,伴不全表现。

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7、

Conclusion: The mode of inheritance of SEDC may be autosomal dominant inheritance.

结论:SEDC遗传方式为常染色体显性遗传。

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8、

RESULTS: Of the family investigated, an autosomal dominant inheritance mode with high penetrance and variable expressivity was suggested.

结果:收集的1个3代非综合征型缺牙家系符合常染色体显性遗传,疾病外显率高,但表现度极不一致。

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9、

Conclusions GEFS~+ is autosomal dominant inheritance disease with conspicuous genetic heterogeneity and phenotypic heterogeneity.

结论GEFS+为常染色体显性遗传性疾病,具有显著遗传异质性和表型异质性。

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10、

From all these characteristics autosomal dominant inheritance was unambiguously established.

上述特征完全符合常染色体显性遗传的特点。

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12、

Sex-limited autosomal dominant inheritance

性限常染色体显性遗传;限性常染色体显性遗传

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13、

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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14、

Owing to the influence of various complex factors, it is possible for the heterozygote of autosomal dominant inheritance to appear in different phenotypes.

由于各种复杂因素的影响,常染色体显性遗传的杂合子有可能出现不同的表现型,本文阐述了常染色体显性遗传的几种类型。

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15、

With pedigree analysis, the genetic mode of the disease in the family are autosomal dominant inheritance.

据系谱分析, 该疾病符合常染色体显性遗传方式.

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16、

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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17、

Conclusion Genetic factors play a major role in the pathogenesis of familial gallstone disease, characterized by autosomal dominant inheritance.

结论(1)家族性胆囊结石病具有常染色体显性遗传特点,遗传因素是发病的基础。

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18、

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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19、

The hereditary APC-R family was identified, and it appeared to manifest autosomal dominant inheritance. 3.

确定为遗传性APC-R家系,符合常染色体显性遗传规律。

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20、

Results ① Three DDEB families are in line with autosomal dominant inheritance;

结果①符合常染色体显性遗传;

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21、

The results of genetic analysis in this disease group suggest that hemochromatosis is an autosomal dominant inheritance but not autosomal recessive inheritance disease.

本组病例遗传方式分析结果,不支持常染色体隐性遗传,确定为常染色体显性遗传。

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22、

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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23、

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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24、

Conclusion The depressed hypoxia response might have been influenced by genetic factors. The model was in accord with autosomal dominant inheritance.

结论低氧呼吸驱动反应性降低可能受遗传因素的影响,且遗传方式符合常染色体显性遗传;

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25、

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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26、

It is obviously autosomal dominant inheritance according to the pedigree.

由于第一代病例仅为右眼虹膜缺损,故较支持中胚层迷走发育的理论。

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28、

The ac2+-Mg2+-ATPase activity of EH patients is distinctly defective and controled by genetic factors and transmitted in autosomal dominant inheritance.

EH患者钙泵活性明显改变,受遗传因素控制,是垂直传递,为常染色体显性遗传。

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29、

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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30、

Objective: To elucidate the molecular mechanism of neurofibromatosis type 2 ( NF2) with autosomal dominant inheritance disease in a Chinese kindred.

目的:探讨中国人常染色体显性遗传2型神经纤维瘤病的基因突变和分子诊断。

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