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.

探索应用引物原位标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.

先性小眼球是一种先异常性眼科疾病,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.

探索应用引物原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性眼科疾病,遗传方式有染色体显性遗传、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.

通常是由同一个体，同一纯种的染色体数目加倍而成的多倍。

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.

先天小眼球是一种先天发育异常眼科疾病,遗传有常染色体显遗传、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的被称为整倍。

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

通常是由同一个体，同一纯种的染色体数目加倍而成的多倍性现。

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

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.

先天性小眼球是一种先天发育异常性眼科疾病,式有常染色体显性、常染色体隐性和X连锁隐性。

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染色非整倍性的靠性。

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,传方式有常染色显性传、常染色隐性传和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，染色数是此种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.

性小眼球是一种育异常性眼科疾病,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.

通常是由同一个，同一纯种的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.

先天性是一种先天发育异常性科疾病,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的现象被称为整倍性。