The genetic analysis shows it is autosomal dominant inheritance.

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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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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They are going to remove into a new building.

他们准备搬进一幢新楼.

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They're going to remove into a new building.

他们准备搬进一座新楼.

《现代汉英综合大词典》

Usually, it is better not remove out outer leaves from fruits and vegetables before storage.

通常最好不要在冷藏前剥去水果和蔬菜上的叶子.

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These circumstances are complained finally company of card remove furniture, make its incur injustice.

这些情况最后都投诉到正牌搬场公司, 使其蒙受不白之冤.

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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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Lipid storage myopathy is one kind of autosomal recessive inherited disease with lipid abnormally sludging in the muscle cell.

脂质沉积性肌病是一种肌细胞内脂肪异常沉积引起的常染色体隐性遗传病。

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WD is a common autosomal recessive inherited neuropathy, whose only pathogenic gene is ATP7B.

WD是神经科较为常见的常染色体隐性遗传病，其唯一致病基因为ATP7B基因。

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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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Parkin is a causative gene of autosomal recessive juvenile parkinsonism.

Parkin是隐性遗传性少年型帕金森病的致病基因。

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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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Citrin deficiency is inherited in an autosomal recessive manner.

希特林缺乏综合征是一种常染色体隐性遗传性疾病。

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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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