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

通是由同一个体，同一纯种的色体数目加而成的现象。

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色体非整的靠。

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眼科疾病,遗传方式有色体显遗传、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.

正状态下，生物体色体数是此种生物单体数目整数的现象被称为整。

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

通常一个体，一纯种的染色体数目加倍而成的多倍现象。

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的靠。

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

先天小眼球一种先天发育异常眼科疾病,方式有常染色体显、常染色体隐和X连锁隐。

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，生物体染色体数此种生物单倍体数目整数倍的现象被称为整倍。

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

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性眼科疾病,遗方式有染色体显性遗、染色体隐性遗和X连锁隐性遗。

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

状态下，生物体染色体数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.

通常是由同一个，同一纯种的染色数目加的多现象。

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非整的靠。

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,遗传方式有常染色遗传、常染色隐遗传和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，生物染色数是此种生物单数目整数的现象被称为整。

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.

探索应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.

先天性小球是一种先天发育异常性病,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，生体染色体数是此种生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.

通常是个体，纯种的染色体数目加倍而成的多倍现象。

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的靠。

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

先天小眼球是种先天发育异常眼科疾病,传方式有常染色体显传、常染色体传和X连锁传。

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。

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

通常是由同一个，同一纯种的色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.

探索应用引原位标记技术分析精子色非整倍性的靠性。

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科疾病,传方式有常色显性传、常色隐性传和X连锁隐性传。

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，生色数是此种生单倍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.

通常是由同一个，同一纯种的色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.

探索应用引原位标记技术分析精子色非整倍性的靠性。

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科疾病,传方式有常色显性传、常色隐性传和X连锁隐性传。

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，生色数是此种生单倍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.

通常是由同一个体，同一纯种的染色体数目加而成的多现象。

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的靠。

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

小眼球是一种发育异常眼科疾病,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数的现象被称为。