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在内含子16内有1个位点存在转换型杂合子。In intron 16 one site has transition heterozygote.

先证者为黎族男青年，属杂合子。The propositus was a young man of Li ethnic group, belonging to heterozygote.

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第二代杂合体自交可以获得纯合体。Finally, the homozygote generation is obtained by self -cross mating of the second heterozygote.

属杂合子常染色体显性遗传性疾病，男性患病率高于女性。Fhcm is a heterozygote autosomal dominant disease and the incidence rate in male is obvious higher than that in female.

属杂合子常染色体显性遗传性疾病，男性患病率高于女性。FHCM is a heterozygote autosomal dominant disease, and the incidence rate in male is obvious higher than that in female.

另外，固定指数分析显示在一些种群和位点有轻微的杂合子缺乏。In addition, analysis of fixation indices revealed a slight heterozygote deficiency in some populations and at some loci.

两对基因都处于杂合状态的个体。相当于复合杂合子。Double heterozygote --- An individual who is heterozygous at each of two different loci. Contrast with compound heterozygote.

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杂合子缺乏会导致某些基因从基因库中消失，造成种群遗传多样性的降低，从而降低物种适应环境的能力。The heterozygote deficiency would result in allele disappear, the lower genetic diversity and the lower ability of adaptation.

结果每个SNP纯合子为单一产物峰，杂合子则为长度不同的两个产物峰。Results For the same SNP locus, the homozygote showed a single product peak, and the heterozygote showed two product peaks with different length.

遗传上已确认为携带特异的突变等位基因，但临床上还未发病的个体。Obligate heterozygote --- An individual who may be clinically unaffected but on the basis of pedigree analysis must carry a specific mutant allele.

由于各种复杂因素的影响，常染色体显性遗传的杂合子有可能出现不同的表现型，本文阐述了常染色体显性遗传的几种类型。Owing to the influence of various complex factors, it is possible for the heterozygote of autosomal dominant inheritance to appear in different phenotypes.

利用杂合子发育过程中来自父本的染色体完全、迅速地消失得到大量单倍体胚。Haploid embryos which only with chromosome of female parent were obtained due to the chromosome elimination of pollen parent quickly and completely during the heterozygote development.

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这类物种的杂交F2群体中杂合子基因型的与一般物种中雌雄个体的减数分裂细胞都发生遗传重组的F2群体杂合子表型不同。The heterozygote genotypes in F2 population in this type of species are different from those in general species in which the genetic recombination occurs in meiosis of both male and female.