The phenomenon, known as Kermodism, is triggered by a recessive mutation at the MC1R gene, the same gene associated with red hair and fair skin in humans.

这种现象称作“卡莫德现象”，是由于MC1R基因发生了隐性突变引发的。

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The experiments of cross and back cross showed that these mutations were belonged to recessive mutation of nucleus gene and controlled by a recessive monogene.

通过正反交试验表明，大豆叶绿素缺失突变属于核基因隐性突变，而且是由一隐性单基因所控制的。

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Because Schinzel-Giedion was already thought to be caused by a DE novo, dominant mutation, narrowing down the list of candidate genes was slightly different than for inherited, recessive disorders.

由于Schinzel - Giedion早已被认为是由新生显性突变引起的，因此缩小候选基因的列表就与隐性遗传疾病略有不同。

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