autosomal的例句大全

Multiple carboxylase deficiency ( MCD) is an autosomal recessive disorder of inherited metabolic diseases.

多种羧化酶缺陷症（MCD）是一种常染色体隐性遗传的先天遗传代谢性疾病。

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The results of segregation analysis indicate that the genetic pattern of UU multiplex families and UA group is autosomal recessive.

分离分析结果显示，U×U多发家庭组和U×A家庭组可以接受常染色体隐性遗传的假设；

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A rare autosomal recessive disease in which the platelets do not produce clots in the normal way and hemorrhage results.

一种罕见的常染色体退缩疾病，症状是血小板不能正常凝固导致流血不止。

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Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation

伴共济失调和智力发育迟缓的常染色体隐性遗传的进行性肌阵挛性癫痫

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A study of DJ-1 gene in 3 pedigrees with autosomal recessive early-onset Parkinson's disease

常染色体隐性遗传早发型帕金森病家系的DJ-1基因研究

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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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β-thalassemia and Spinal muscular atrophy ( SMA) are two common autosomal recessive diseases.

β地中海贫血和脊髓性肌萎缩是两种常见的单基因遗传病。

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It is a common occurrence in dogs and is thought to be a sex-limited autosomal recessive trait.

该疾病常发于犬，并被认为具有限性常染色体隐性遗传特征。

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The recurrence risk for this disease is, of course, 25% because of the autosomal recessive inheritance pattern.

因为它是常染色体隐性遗传的，所以它在家族中的发病率是25%。

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Autosomal recessive polycystic kidnay disease: clinical, pathological and radiological correlations

常染色体隐性遗传性多囊肾病：临床、病理与影像学表现

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Wilson ′ s disease is a autosomal recessive inherited disease characteristic by metabolic disorder of copper.

肝豆状核变性是一种铜代谢障碍的常染色体隐性遗传病。

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Objective To explore the clinical features of autosomal recessive juvenile Parkinson disease ( AR-JP).

目的探讨常染色体隐性遗传性青少年型帕金森病（AR-JP）的临床特征。

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The Proportion and Clinical Feature of Duchenne Muscular Dystrophy With Autosomal Recessive Inheritance

常染色体隐性遗传的类Duchenne肌营养不良临床特征及其发生比率的估计值分析

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Genotype and phenotype analyses of three families with autosomal recessive juvenile parkinsonism

三个常染色体隐性遗传性青少年型帕金森综合征家系的基因型与表型分析

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Autosomal recessive inheritance was difficult to be evaluated because of few families remained.

常染色体隐性遗传因剩下的家系样本太少，难以预测；

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TH gene mutation in Chinese patients with autosomal recessive dopa-responsive dystonia

中国人常染色体隐性遗传性多巴反应性肌张力障碍TH基因突变分析

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This mutation appears to be unique to Chinese population, and may follow autosomal recessive inheritance.

该突变可能是中国人群独有的突变。

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