Heterozygous mutations were identified in 12 of 13 tumors.
13例肿瘤中有12例发现杂合子突变。
Haired heterozygous mice possess normal reproductive capability.
杂合子有毛小鼠的生育能力正常。
Conclusions Novel compound heterozygous nonsense mutation of KCNQ1 can cause JLNS.
结论JLNS可由KCNQ1基因上复合的杂合突变所引起。
Methods: nine heterozygous mutation carriers and nine healthy controls were investigated.
方法：调查9名杂合子突变携带者和9名健康对照者。
The advantage and constraints of the double heterozygous loci mapping strategy was discussed.
本文对所提出的利用双杂合位点构建果树遗传图谱的策略进行了讨论。
Conclusion a new compound heterozygous mutation of ECM1 gene was identified in this LP family.
结论本类脂质蛋白沉积症家系存在新的ECM 1基因突变位点。
In genetics, refers to an allele that is expressed in both the heterozygous and homozygous condition.
指等位基因在杂合状态和纯合状态都有表达的现象。
A large family of children all showed the same fingerprint (heterozygous) for D1S80. how is this possible?
一个大家庭的儿童均表现出相同的指纹档(杂合子)的D1S80。怎么可能？
White male butterflies, most of which are heterozygous at the gene that controls color, show no color preference.
而大多数的白色蝴蝶在颜色决定基因上是杂合的，因此不具有求偶上的颜色偏好。
Conclusion Inherited afibrinogenemia is caused by the compound heterozygous deletion in the fibrinogen FGA gene.
结论纤维蛋白原FGA基因复合杂合缺失是引起该家系先证者无纤维蛋白原血症的原因。
Conclusion The proband's hearing loss resulted from the compound heterozygous mutations N392Y and S448X for SLC26A4 gene.
结论SLC26A4基因的N392Y、S448X复合杂合突变是导致该先证者耳聋发生的原因。
RESULTS: The final accuracy for homozygous and heterozygous single-nucleotide polymorphisms reached 99.62% and 98.39%, respectively.
结果显示，纯合子和杂合子的单核苷酸多态性的最终精度分别达到99.62%和98.39%。
This locus occurs in over 40% of the population and is associated with increased risk of 40% in homozygous and 15 to 20% in heterozygous.
该位点出现在40%以上的人群中，其与纯合子风险增大40%以及杂合子风险增大20%的现象相关。
The main causes resulting in poor anther dehiscence in hybrid F1 were different with the kind and the number of heterozygous pollen sterility loci.
杂种f 1花药不开裂的原因随其所含的杂合花粉不育基因座位种类和数目不同而异。
SCAR this study used molecular markers for the identification of heterozygous that SCAR marker than other molecular markers more reliable and stable.
本研究采用SCAR分子标记进行杂合子的鉴定，证明scar标记较其他分子标记更加可靠和稳定。
On the one hand, searching for heterozygous variants can be slightly trickier, said Veltman, because individuals have many more heterozygous variants than homozygous.
一方面，Veltman表示，寻找杂合变异体要略微棘手一些，因为个体携带的杂合变异体比纯合变异体要多得多。
A variety of approaches have been used to address this issue, the most common of which is the study of tumors in women, who are heterozygous for X-linked marker enzymes.
一系列的方法已被用来探讨这个问题，其中一个最常用的方法是研究女性肿瘤，她们是X连锁标记酶杂合子。
Results a homozygous mutation at exon 13 of the proband was found by parallel TGGE. Homozygous and heterozygous mutations were also found in the family by parallel TGGE.
结果平行tgge发现，两患儿第13外显子存在一纯合突变，其父母此外显子存在杂合突变。
Instead of looking for homozygous variants where each parent carried an allele, the researchers were looking for heterozygous variants that were also not present in the parents.
研究人员寻找不存在与父母中的杂合变异体，而不是寻找每位亲本携带一个等位基因的纯合变异体。
Heterozygous type I (quantitative) and most type II (qualitative) antithrombin deficiencies highly increase the risk of venous thromboembolism (VTE), while homozygous mutations are lethal.
杂合子i型(定量)和大多数II型(定性)抗凝血酶缺乏症使静脉血栓栓塞(VTE)的风险显着增加，而纯合型突变会导致死亡。
Heterozygous type I (quantitative) and most type II (qualitative) antithrombin deficiencies highly increase the risk of venous thromboembolism (VTE), while homozygous mutations are lethal.
杂合子i型(定量)和大多数II型(定性)抗凝血酶缺乏症使静脉血栓栓塞(VTE)的风险显着增加，而纯合型突变会导致死亡。
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