Autopolyploidy A type of polyploidy involving the multiplication of chromo-some sets from only one species.

通常是由同一个，同一纯种数目加倍而倍性现象。

Objective: To explore the reliability of the method PRINS for detection of spermic aneuploidy.

探索应用引物原位标记技术分析精子非整倍性靠性。

Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.

先天性小眼球是一种先天发育异常性眼科疾病,遗传方式有常显性遗传、常隐性遗传和X连锁隐性遗传。

Euploidy The normal state in which an organism's chromosome number is an exact multiple of the haploid number characteristic of the species.

正常状态下，生物数是此种生物单倍数目整数倍现象被称为整倍性。

Autopolyploidy A type of polyploidy involving the multiplication of chromo-some sets from only one species.

通常是由同一个，同一纯种数目加倍而成多倍性现象。

Objective: To explore the reliability of the method PRINS for detection of spermic aneuploidy.

探索应用引物原位标记技术分析精子非整倍性靠性。

Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.

先天性小眼球是一种先天发育异常性眼科疾病,遗传方式有常显性遗传、常性遗传和X连锁性遗传。

Euploidy The normal state in which an organism's chromosome number is an exact multiple of the haploid number characteristic of the species.

正常状态下，生物数是此种生物单倍数目整数倍现象被称为整倍性。

Autopolyploidy A type of polyploidy involving the multiplication of chromo-some sets from only one species.

通常是由同一个体，同一纯种染色体数目加倍而成多倍现象。

Objective: To explore the reliability of the method PRINS for detection of spermic aneuploidy.

探索应用引物原位标记技术分析精子染色体非整倍。

Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.

先天小眼球是一种先天发育异常眼科疾病,遗传方式有常染色体显遗传、常染色体隐遗传和X连锁隐遗传。

Euploidy The normal state in which an organism's chromosome number is an exact multiple of the haploid number characteristic of the species.

正常状态下，生物体染色体数是此种生物单倍体数目整数倍现象被称为整倍。

Autopolyploidy A type of polyploidy involving the multiplication of chromo-some sets from only one species.

通常是由同一个体，同一纯种染色体数目加而成多现象。

Objective: To explore the reliability of the method PRINS for detection of spermic aneuploidy.

探索应用引物原位标记技术分析精子染色体非整。

Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.

天小眼球是一种天发育异常眼科疾病,遗传方式有常染色体显遗传、常染色体隐遗传和X连锁隐遗传。

Euploidy The normal state in which an organism's chromosome number is an exact multiple of the haploid number characteristic of the species.

正常状态下，生物体染色体数是此种生物单体数目整数现象被称为整。

Autopolyploidy A type of polyploidy involving the multiplication of chromo-some sets from only one species.

通常是由同一个，同一纯种数目加倍而成多倍性现象。

Objective: To explore the reliability of the method PRINS for detection of spermic aneuploidy.

探索应用引物原位标记技术分析精子非整倍性靠性。

Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.

先天性小眼球是一种先天发育异常性眼科疾病,遗传方式有常显性遗传、常性遗传和X连锁性遗传。

Euploidy The normal state in which an organism's chromosome number is an exact multiple of the haploid number characteristic of the species.

正常状态下，生物数是此种生物单倍数目整数倍现象被称为整倍性。

Autopolyploidy A type of polyploidy involving the multiplication of chromo-some sets from only one species.

通常是由同一个体，同一纯种的染色体数目加倍而成的多倍性现象。

Objective: To explore the reliability of the method PRINS for detection of spermic aneuploidy.

探索物原位标记技术分析精子染色体非整倍性的靠性。

Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.

先天性小眼球是一种先天发育异常性眼,遗传方式有常染色体显性遗传、常染色体隐性遗传和X连锁隐性遗传。

Euploidy The normal state in which an organism's chromosome number is an exact multiple of the haploid number characteristic of the species.

正常状态下，生物体染色体数是此种生物单倍体数目整数倍的现象被称为整倍性。

Autopolyploidy A type of polyploidy involving the multiplication of chromo-some sets from only one species.

通常由同一个体，同一纯种的染色体目加倍而成的多倍性现象。

Objective: To explore the reliability of the method PRINS for detection of spermic aneuploidy.

探索应用引物原位标记技术分析精子染色体非整倍性的靠性。

Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.

先天性小眼球一种先天发育异常性眼科疾病,遗传方式有常染色体显性遗传、常染色体隐性遗传和X连锁隐性遗传。

Euploidy The normal state in which an organism's chromosome number is an exact multiple of the haploid number characteristic of the species.

正常状态下，生物体染色体种生物单倍体目整倍的现象被称为整倍性。

Autopolyploidy A type of polyploidy involving the multiplication of chromo-some sets from only one species.

通常由同一个体，同一纯种的染色体目加倍而成的多倍性现象。

Objective: To explore the reliability of the method PRINS for detection of spermic aneuploidy.

探索应用引物原位标记技术分析精子染色体非整倍性的靠性。

Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.

先天性小眼球一种先天发育异常性眼科疾病,遗传方式有常染色体显性遗传、常染色体隐性遗传和X连锁隐性遗传。

Euploidy The normal state in which an organism's chromosome number is an exact multiple of the haploid number characteristic of the species.

正常状态下，生物体染色体种生物单倍体目整倍的现象被称为整倍性。

Autopolyploidy A type of polyploidy involving the multiplication of chromo-some sets from only one species.

通是由同一个，同一纯种的目加倍而成的多倍性现象。

Objective: To explore the reliability of the method PRINS for detection of spermic aneuploidy.

探索应用引物原位标记技术分析精子非整倍性的靠性。

Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.

先天性小眼球是一种先天发育异性眼科疾病,遗传方式有显性遗传、隐性遗传和X连锁隐性遗传。

Euploidy The normal state in which an organism's chromosome number is an exact multiple of the haploid number characteristic of the species.

正状态下，生物是此种生物单倍目整倍的现象被称为整倍性。