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.

先天性小眼球是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，物体染色体数是此种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.

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,方式有常染色体显性、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现象。

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

探索应用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.

先天小球是一种先天发育异常疾病,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。

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现象。

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

探索应用引物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眼科疾病,遗传方式有染色体显遗传、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.

通常由同个体，同纯种的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.

先天性小眼种先天发育异常性眼科疾病,遗传方式有常色体显性遗传、常色体隐性遗传和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,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，体染色体数是此种单倍体数目整数倍的现象被称为整倍性。