PARK 6具有临床异质性。
PARK2和PARK6具有相似临床表现，但均具有临床异质性。
PARK2 and PARK6 should have the similar clinical features, but all have clinical heterogeneity.
临床异质性，诊断标准，方法的遗传风险估计，观点的预防这种疾病进行了讨论。
The clinical heterogeneity, diagnostic criteria, methods of genetic risk estimation, perspectives of prevention of this disease are discussed.
不同基因型决定相同表型的现象。参见等位基因异质性、临床异质性和基因座异质性。
Genetic lethal --- A mutant allele or genetically determined trait that leads to failure to reproduce, although not necessarily to death prior to reproduction.
因为，HSP是一组具有明显临床和遗传异质性的疾病，临床诊断和分型有一定的困难。
It is difficult to have a diagnosis of HSP for HSP is a clinically and genetically heterogeneous group of disorders.
背景：血小板对氯吡格雷的反应性存在异质性，而且以氯砒格雷作为次选血小板抑制剂的临床或生物化学预测尚不清楚。
Background: a heterogeneous platelet reactivity response to clopidogrel exists, and the clinical or biochemical predictors of suboptimal PI with clopidogrel remain unclear.
我们调查了HER 2异质性对112例her 2阳性转移性乳腺癌患者的曲妥珠单抗疗效和临床预后的影响。
We investigated the impact of HER2 heterogeneity on trastuzumab responses and clinical outcomes in 112 patients with HER2-positive metastatic breast cancer.
目的：评价头孢西丁扩散法检测耐甲氧西林葡萄球菌异质性耐药菌株的可靠性和临床实用性。
Objective To evaluate the reliability and clinical practicability of cefoxitin disk diffusion test in the detection of methicillin-resistant staphylococcus (MRS) heterogenic drug-resistant strains.
该疾病的临床表现具有一定的异质性。
The clinical manifestations of the disease are very heterogeneity.
TSA中临床病理和分子特征方面的异质性与癌前病变的状态或类型相关。
The heterogeneity of TSAs in terms of clinicopathologic and molecular features correlated with the status or type of precursor lesions.
临床表型存在高度的异质性，是否与生活习惯或基因多态性有关有待进一步研究。
Further study is warranted to investigate the association of this heterogeneity with lifestyle or genetic information.
HHV8相关淋巴瘤可能具有临床表现和病理形态的异质性，其某些特征可能导致误诊为其它类型的淋巴瘤。
HHV8-associated lymphomas can be clinically and pathologically heterogeneous, with features that may lead to misdiagnosis as other types of lymphoma.
基于发表的文献，提供了有关基因座异质性、突变类型、临床和生化数据、地理位置和常见突变的信息。
Information on locus heterogeneity, type of mutation, clinical and biochemical data, geographical location and common mutations are furnished based on published literature.
该位点基因突变异质性水平与亲缘关系、抽搐发作的早现性和血浆乳酸检测值等临床表型存在相关性。
The mutant heteroplasmy levels are positively associated with genetic relationship, seizure anticipation, plasma lactate data and other clinical features.
目的采用循证医学的方法对超声造影诊断肝局灶性结节增生的研究进行系统评价，评估其临床应用价值并分析异质性来源。
Objective A systematic review was conducted to determine reliability of contrast-enhanced ultrasonography diagnostic tests for focal nodular hyperplasia and to explore sources of heterogeneity.
目的采用循证医学的方法对超声造影诊断肝局灶性结节增生的研究进行系统评价，评估其临床应用价值并分析异质性来源。
Objective A systematic review was conducted to determine reliability of contrast-enhanced ultrasonography diagnostic tests for focal nodular hyperplasia and to explore sources of heterogeneity.
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