All of these recessive mutations, which are considered to be null alleles, exhibit defects in internode elongation.
被认为是无效等位基因的这些隐性突变都存在节间伸长缺陷。
It was shown that temporary stopping of shops led to a decrease in the number of recessive mutations in CSN to the level 1.5 times higher than the control one.
结果表明，临时停车的商店导致的数量减少隐性突变的国别战略，以1.5倍的水平高于对照1。
Recessive mutations in several loci of Arabidopsis were previously shown to lead to a collapsed xylem phenotype but water-transport deficiency was not observed.
以前发现的拟南芥中几个位点的隐性突变导致了木质部萎陷的表型，但没有观察到水分运输的缺失。
This apparent anomaly is partially explained by the fact that most founder mutations are recessive: only a person with copies of the affected gene from both parents becomes ill.
大多数明显的创始人突变都是隐性的，可以解释这种明显的异常现象：只有双亲都拥有受影响基因副本的人才会生病。
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。
Conclusion the mutations in GJB2 are the major cause of prelingual deafness; two causative mutations can be found in (28.6%) prelingual recessive and in (18.9%) prelingual sporadic NSHL patients.
结论GJB2突变是导致学语前聋的主要原因，28.6%的学语前隐性和18.9%学语前散发非综合征性耳聋病人携带了两个GJB2突变。
The research team says that the gene therapy might also be used in treating recessive and dominant forms of cone-rod dystrophy (CORD) caused by mutations in GUCY2D.
该研究小组说，基因疗法还可能用于治疗GUCY2D的突变引起的锥杆营养不良（线）的隐性和显性的形式。
Mutations in HFM1 in recessive primary ovarian insufficiency.
【译】在原发性卵巢功能不全在hfm1隐性突变。
Treating the PDE6B-mutant mouse model is important, because as much as five percent of people with recessive RP have mutations in PDE6B.
治疗PDE6B突变体小鼠模型是重要的，因为多达五种具有隐性RP的民众在PDE6B突变。
Mutations in the mitochondrial PTEN-induced kinase 1 cause early onset recessive Parkinson's.
线粒体中pten引起的激酶1的突变会引起早发型阿尔茨海默病。
Mutations in the corresponding ATM gene result in ataxia telangiectasia (at), an autosomal recessive disease characterized by uncoordinated muscle movement and neurodegeneration.
AT M基因突变可导致共济失调毛细血管扩张症(AT)，一种常染色体隐性遗传病，该病特点是不协调的肌肉运动和神经退化。
Mutations in the corresponding ATM gene result in ataxia telangiectasia (at), an autosomal recessive disease characterized by uncoordinated muscle movement and neurodegeneration.
AT M基因突变可导致共济失调毛细血管扩张症(AT)，一种常染色体隐性遗传病，该病特点是不协调的肌肉运动和神经退化。
应用推荐