autosomal dominant inheritance

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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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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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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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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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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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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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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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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The transmission accords with autosomal dominant inheritance.

符合常染色体显性遗传。

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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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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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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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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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Inherited style of primary hypertension was not autosomal dominant inheritance are autosomal recessive inheritance.

不属于常染色体显性或隐性遗传方式。

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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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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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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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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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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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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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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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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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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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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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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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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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Although previous hybridization tests proved that polydactyly trait belonged with an autosomal dominant inheritance but the penetrance is difference in offspring populations.

已有杂交试验证明鸡多趾性状为常染色体显性遗传但外显率不同。

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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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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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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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