Chromosomes also determine the sex of animals.

色体也决定动物的性别。

Maple tree saccharorrhea sickness belongs to the euchromosome recessive hereditary disease.

枫糖尿症属于常色体隐性遗传病。

The polytene chromosomes found in the salivary gland cells are among the largest chromosomes known today.

唾液腺细胞中的多线色体是目前已知的最大色体一。

The polymorphy of fronds and chromosome number of Ophioglossum petiolatum Hook.

有梗瓶尔小草叶的多形性和色体数目.

If both of a pair of homologous chromosomes are missing, nullisomy results.

如果一对同源色体都缺失了，称为缺体。

Y chromosome has two types of polymorphism:metacentric (or submetacentric) and acrocentric chromosomes.

色体有中部(或亚中部)和近端着色体。

Lysogeny is a semi-permanent association between the phage and host chromosomes.

溶源性是噬菌体和寄生色体间的半永久联合。

This paper summarizes the roles of minichromosome maintenace proteins in DNA replication.

本文就微小色体白在复制中的作用简单综述。

About 1 in every 700 babies has this exbert cuppy, the extra copy.

每700个婴儿中就有1个会有这多余的一条色体。

Dynein also helps force apart chromosomes during cell division.

以及在细胞分裂中，提供了机械能协助色体的分离。”

In the nucleoplasm chromosomes consisting of deoxyribonucleic acid (DNA) and proteins are present.

核质中的色体由脱氧核糖核酸（DNA）和白质构成。

A case of trisomy 22 liveborn female baby with multiple congenital anomalies is described.

摘要作者报告一例具有多种先天性异常的三色体22症的活产女婴。

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

通常是由同一个体，同一纯种的色体数目加倍而成的多倍性现象。

Dentinogenesis imperfecta (DI) is a kind of mesodermal defect inherited in a simple autosomal dominant mode.

摘要牙本质形成不良是一种体色体显性遗传的中胚层缺陷。

Objective: Improve and optimize the method of Chromosome of zooblast.

改进和优化动物细胞色体的临时制片技术。

Methods :Using the chromo somal analysis and flurospectrop hotomytry methods to expel the chromosomal abnormality and mucoplysacch aridosis.

方法色体检查排除色体病,采用荧光光度计检测。

Conclusion Sauropus androgynus has certain genetic toxicity of chromosomal aberration induction and its molecular mechanism needs further investigation.

结论守宫木具有一定的诱发色体畸变的遗传毒性。

In plants this is sometimes overcome by the doubling of the chromosome number, giving an allopolyploid.

在植物中，这种不育现象有时可因为色体数目加倍而抵消，产生同源多倍体。

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倍性的可靠性。

Chromomere A small beadlike deeply staining structure seen in chromosomes during prophase of mitosis and meiosis.

在有分裂及减数分裂的前期存在于色体上的小念珠状的着色深的结构。

Chromosomes also determine the sex of animals.

染色体也决定动物的性别。

Maple tree saccharorrhea sickness belongs to the euchromosome recessive hereditary disease.

枫糖尿症属于常染色体隐性遗传病。

The polytene chromosomes found in the salivary gland cells are among the largest chromosomes known today.

唾液腺细胞中的多线染色体是目前已知的最大染色体。

The polymorphy of fronds and chromosome number of Ophioglossum petiolatum Hook.

有梗瓶尔小草叶的多形性和染色体数目.

If both of a pair of homologous chromosomes are missing, nullisomy results.

如果对源染色体都缺失了，称为缺体。

Y chromosome has two types of polymorphism:metacentric (or submetacentric) and acrocentric chromosomes.

染色体有中部(或亚中部)和近端着丝粒染色体。

Lysogeny is a semi-permanent association between the phage and host chromosomes.

溶源性是噬菌体和寄染色体间的半永久联合。

This paper summarizes the roles of minichromosome maintenace proteins in DNA replication.

本文就微小染色体维持蛋白在复制中的作用简单综述。

About 1 in every 700 babies has this exbert cuppy, the extra copy.

每700个婴儿中就有1个会有这多余的条染色体。

Dynein also helps force apart chromosomes during cell division.

以及在细胞分裂中，提供了机械能协助染色体的分离。”

In the nucleoplasm chromosomes consisting of deoxyribonucleic acid (DNA) and proteins are present.

核质中的染色体脱氧核糖核酸（DNA）和蛋白质构成。

A case of trisomy 22 liveborn female baby with multiple congenital anomalies is described.

摘要作者报告例具有多种先天性异常的三染色体22症的活产女婴。

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性现象。

Dentinogenesis imperfecta (DI) is a kind of mesodermal defect inherited in a simple autosomal dominant mode.

摘要牙本质形成不良是种体染色体显性遗传的中胚层缺陷。

Objective: Improve and optimize the method of Chromosome of zooblast.

改进和优化动物细胞染色体的临时制片技术。

Methods :Using the chromo somal analysis and flurospectrop hotomytry methods to expel the chromosomal abnormality and mucoplysacch aridosis.

方法染色体检查排除染色体病,采用荧光光度计检测。

Conclusion Sauropus androgynus has certain genetic toxicity of chromosomal aberration induction and its molecular mechanism needs further investigation.

结论守宫木具有定的诱发染色体畸变的遗传毒性。

In plants this is sometimes overcome by the doubling of the chromosome number, giving an allopolyploid.

在植物中，这种不育现象有时可因为染色体数目加倍而抵消，产源多倍体。

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可靠性。

Chromomere A small beadlike deeply staining structure seen in chromosomes during prophase of mitosis and meiosis.

在有丝分裂及减数分裂的前期存在于染色体上的小念珠状的着色深的结构。

Chromosomes also determine the sex of animals.

染色体也决定动物性别。

Maple tree saccharorrhea sickness belongs to the euchromosome recessive hereditary disease.

枫糖尿症属于常染色体隐性遗传病。

The polytene chromosomes found in the salivary gland cells are among the largest chromosomes known today.

唾液腺细胞多线染色体是目前已知最大染色体一。

The polymorphy of fronds and chromosome number of Ophioglossum petiolatum Hook.

有梗瓶尔小草叶多形性染色体数目.

If both of a pair of homologous chromosomes are missing, nullisomy results.

如果一对同源染色体都缺失了，称为缺体。

Y chromosome has two types of polymorphism:metacentric (or submetacentric) and acrocentric chromosomes.

染色体有(或亚)近端着丝粒染色体。

Lysogeny is a semi-permanent association between the phage and host chromosomes.

溶源性是噬菌体寄生染色体间半永久联合。

This paper summarizes the roles of minichromosome maintenace proteins in DNA replication.

本文就微小染色体维持蛋白在复作用简单综述。

About 1 in every 700 babies has this exbert cuppy, the extra copy.

每700个婴儿就有1个会有这多余一条染色体。

Dynein also helps force apart chromosomes during cell division.

以及在细胞分裂，提供了机械能协助染色体分离。”

In the nucleoplasm chromosomes consisting of deoxyribonucleic acid (DNA) and proteins are present.

核质染色体由脱氧核糖核酸（DNA）蛋白质构成。

A case of trisomy 22 liveborn female baby with multiple congenital anomalies is described.

摘要作者报告一例具有多种先天性异常三染色体22症活产女婴。

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性现象。

Dentinogenesis imperfecta (DI) is a kind of mesodermal defect inherited in a simple autosomal dominant mode.

摘要牙本质形成不良是一种体染色体显性遗传胚层缺陷。

Objective: Improve and optimize the method of Chromosome of zooblast.

改进优化动物细胞染色体临时片技术。

Methods :Using the chromo somal analysis and flurospectrop hotomytry methods to expel the chromosomal abnormality and mucoplysacch aridosis.

方法染色体检查排除染色体病,采用荧光光度计检测。

Conclusion Sauropus androgynus has certain genetic toxicity of chromosomal aberration induction and its molecular mechanism needs further investigation.

结论守宫木具有一定诱发染色体畸变遗传毒性。

In plants this is sometimes overcome by the doubling of the chromosome number, giving an allopolyploid.

在植物，这种不育现象有时可因为染色体数目加倍而抵消，产生同源多倍体。

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可靠性。

Chromomere A small beadlike deeply staining structure seen in chromosomes during prophase of mitosis and meiosis.

在有丝分裂及减数分裂前期存在于染色体上小念珠状着色深结构。

Chromosomes also determine the sex of animals.

体也决定动物性别。

Maple tree saccharorrhea sickness belongs to the euchromosome recessive hereditary disease.

枫糖尿症属于常体隐性遗传病。

The polytene chromosomes found in the salivary gland cells are among the largest chromosomes known today.

唾液腺细胞中多线体是目最大体一。

The polymorphy of fronds and chromosome number of Ophioglossum petiolatum Hook.

有梗瓶尔小草叶多形性和体数目.

If both of a pair of homologous chromosomes are missing, nullisomy results.

如果一对同源体都缺失了，称为缺体。

Y chromosome has two types of polymorphism:metacentric (or submetacentric) and acrocentric chromosomes.

体有中部(或亚中部)和近端着丝粒体。

Lysogeny is a semi-permanent association between the phage and host chromosomes.

溶源性是噬菌体和寄生体间半永久联合。

This paper summarizes the roles of minichromosome maintenace proteins in DNA replication.

本文就微小体维持蛋白在复制中作用简单综述。

About 1 in every 700 babies has this exbert cuppy, the extra copy.

每700个婴儿中就有1个会有这多余一条体。

Dynein also helps force apart chromosomes during cell division.

以及在细胞分裂中，提供了机械能协助体分离。”

In the nucleoplasm chromosomes consisting of deoxyribonucleic acid (DNA) and proteins are present.

核质中体由脱氧核糖核酸（DNA）和蛋白质构成。

A case of trisomy 22 liveborn female baby with multiple congenital anomalies is described.

摘要作者报告一例具有多种先天性异常三体22症活产女婴。

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

通常是由同一个体，同一纯种体数目加倍而成多倍性现象。

Dentinogenesis imperfecta (DI) is a kind of mesodermal defect inherited in a simple autosomal dominant mode.

摘要牙本质形成不良是一种体体显性遗传中胚层缺陷。

Objective: Improve and optimize the method of Chromosome of zooblast.

改进和优化动物细胞体临时制片技术。

Methods :Using the chromo somal analysis and flurospectrop hotomytry methods to expel the chromosomal abnormality and mucoplysacch aridosis.

方法体检查排除体病,采用荧光光度计检测。

Conclusion Sauropus androgynus has certain genetic toxicity of chromosomal aberration induction and its molecular mechanism needs further investigation.

结论守宫木具有一定诱发体畸变遗传毒性。

In plants this is sometimes overcome by the doubling of the chromosome number, giving an allopolyploid.

在植物中，这种不育现象有时可因为体数目加倍而抵消，产生同源多倍体。

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体非整倍性可靠性。

Chromomere A small beadlike deeply staining structure seen in chromosomes during prophase of mitosis and meiosis.

在有丝分裂及减数分裂期存在于体上小念珠状着深结构。

Chromosomes also determine the sex of animals.

染色也决定动物的性别。

Maple tree saccharorrhea sickness belongs to the euchromosome recessive hereditary disease.

枫糖尿症属于常染色隐性遗传病。

The polytene chromosomes found in the salivary gland cells are among the largest chromosomes known today.

唾液腺细胞中的多线染色是目前已知的最大染色一。

The polymorphy of fronds and chromosome number of Ophioglossum petiolatum Hook.

有梗瓶尔小草叶的多形性和染色数目.

If both of a pair of homologous chromosomes are missing, nullisomy results.

如果一对同源染色失了，称为。

Y chromosome has two types of polymorphism:metacentric (or submetacentric) and acrocentric chromosomes.

染色有中部(或亚中部)和近端着丝粒染色。

Lysogeny is a semi-permanent association between the phage and host chromosomes.

溶源性是噬菌和寄生染色间的半永久联合。

This paper summarizes the roles of minichromosome maintenace proteins in DNA replication.

本文就微小染色维持蛋白在复制中的作用简单综述。

About 1 in every 700 babies has this exbert cuppy, the extra copy.

每700个婴儿中就有1个有多余的一条染色。

Dynein also helps force apart chromosomes during cell division.

以及在细胞分裂中，提供了机械能协助染色的分离。”

In the nucleoplasm chromosomes consisting of deoxyribonucleic acid (DNA) and proteins are present.

核质中的染色由脱氧核糖核酸（DNA）和蛋白质构成。

A case of trisomy 22 liveborn female baby with multiple congenital anomalies is described.

摘要作者报告一例具有多种先天性异常的三染色22症的活产女婴。

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。

Dentinogenesis imperfecta (DI) is a kind of mesodermal defect inherited in a simple autosomal dominant mode.

摘要牙本质形成不良是一种染色显性遗传的中胚层陷。

Objective: Improve and optimize the method of Chromosome of zooblast.

改进和优化动物细胞染色的临时制片技术。

Methods :Using the chromo somal analysis and flurospectrop hotomytry methods to expel the chromosomal abnormality and mucoplysacch aridosis.

方法染色检查排除染色病,采用荧光光度计检测。

Conclusion Sauropus androgynus has certain genetic toxicity of chromosomal aberration induction and its molecular mechanism needs further investigation.

结论守宫木具有一定的诱发染色畸变的遗传毒性。

In plants this is sometimes overcome by the doubling of the chromosome number, giving an allopolyploid.

在植物中，种不育现象有时可因为染色数目加倍而抵消，产生同源多倍。

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非整倍性的可靠性。

Chromomere A small beadlike deeply staining structure seen in chromosomes during prophase of mitosis and meiosis.

在有丝分裂及减数分裂的前期存在于染色上的小念珠状的着色深的结构。

Chromosomes also determine the sex of animals.

体也决定动物的性别。

Maple tree saccharorrhea sickness belongs to the euchromosome recessive hereditary disease.

枫糖尿症属于常体隐性遗传病。

The polytene chromosomes found in the salivary gland cells are among the largest chromosomes known today.

唾液腺细胞中的多线体是目前已知的最大体。

The polymorphy of fronds and chromosome number of Ophioglossum petiolatum Hook.

有梗瓶尔小草叶的多形性和体数目.

If both of a pair of homologous chromosomes are missing, nullisomy results.

如同源体都缺失了，称为缺体。

Y chromosome has two types of polymorphism:metacentric (or submetacentric) and acrocentric chromosomes.

体有中部(或亚中部)和近端着丝粒体。

Lysogeny is a semi-permanent association between the phage and host chromosomes.

溶源性是噬菌体和寄生体间的半永久联合。

This paper summarizes the roles of minichromosome maintenace proteins in DNA replication.

本文就微小体维持蛋白在复制中的作用简单综述。

About 1 in every 700 babies has this exbert cuppy, the extra copy.

每700个婴儿中就有1个会有这多余的体。

Dynein also helps force apart chromosomes during cell division.

以及在细胞分裂中，提供了机械能协助体的分离。”

In the nucleoplasm chromosomes consisting of deoxyribonucleic acid (DNA) and proteins are present.

核质中的体由脱氧核糖核酸（DNA）和蛋白质构成。

A case of trisomy 22 liveborn female baby with multiple congenital anomalies is described.

摘要作者报告例具有多种先天性异常的三体22症的活产女婴。

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

通常是由同个体，同纯种的体数目加倍而成的多倍性现象。

Dentinogenesis imperfecta (DI) is a kind of mesodermal defect inherited in a simple autosomal dominant mode.

摘要牙本质形成不良是种体体显性遗传的中胚层缺陷。

Objective: Improve and optimize the method of Chromosome of zooblast.

改进和优化动物细胞体的临时制片技术。

Methods :Using the chromo somal analysis and flurospectrop hotomytry methods to expel the chromosomal abnormality and mucoplysacch aridosis.

方法体检查排除体病,采用荧光光度计检测。

Conclusion Sauropus androgynus has certain genetic toxicity of chromosomal aberration induction and its molecular mechanism needs further investigation.

结论守宫木具有定的诱发体畸变的遗传毒性。

In plants this is sometimes overcome by the doubling of the chromosome number, giving an allopolyploid.

在植物中，这种不育现象有时可因为体数目加倍而抵消，产生同源多倍体。

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体非整倍性的可靠性。

Chromomere A small beadlike deeply staining structure seen in chromosomes during prophase of mitosis and meiosis.

在有丝分裂及减数分裂的前期存在于体上的小念珠状的着深的结构。

Chromosomes also determine the sex of animals.

色体也决定性别。

Maple tree saccharorrhea sickness belongs to the euchromosome recessive hereditary disease.

枫糖尿症属于常色体隐性遗传病。

The polytene chromosomes found in the salivary gland cells are among the largest chromosomes known today.

唾液腺细胞中多线色体是目前已知最大色体一。

The polymorphy of fronds and chromosome number of Ophioglossum petiolatum Hook.

有梗瓶尔小草叶多形性和色体数目.

If both of a pair of homologous chromosomes are missing, nullisomy results.

如果一对同源色体都缺失了，称为缺体。

Y chromosome has two types of polymorphism:metacentric (or submetacentric) and acrocentric chromosomes.

色体有中部(或亚中部)和近端着丝粒色体。

Lysogeny is a semi-permanent association between the phage and host chromosomes.

溶源性是噬菌体和寄生色体间半永久联合。

This paper summarizes the roles of minichromosome maintenace proteins in DNA replication.

本文就微小色体维持蛋白在复制中作用简单综述。

About 1 in every 700 babies has this exbert cuppy, the extra copy.

每700个婴儿中就有1个会有这多余一条色体。

Dynein also helps force apart chromosomes during cell division.

以及在细胞分裂中，提供了机械能协助色体分离。”

In the nucleoplasm chromosomes consisting of deoxyribonucleic acid (DNA) and proteins are present.

核质中色体由脱氧核糖核酸（DNA）和蛋白质构成。

A case of trisomy 22 liveborn female baby with multiple congenital anomalies is described.

摘要作者报告一例具有多种先天性异常色体22症活产女婴。

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

通常是由同一个体，同一纯种色体数目加倍而成多倍性现象。

Dentinogenesis imperfecta (DI) is a kind of mesodermal defect inherited in a simple autosomal dominant mode.

摘要牙本质形成不良是一种体色体显性遗传中胚层缺陷。

Objective: Improve and optimize the method of Chromosome of zooblast.

改进和优化细胞色体临时制片技术。

Methods :Using the chromo somal analysis and flurospectrop hotomytry methods to expel the chromosomal abnormality and mucoplysacch aridosis.

方法色体检查排除色体病,采用荧光光度计检测。

Conclusion Sauropus androgynus has certain genetic toxicity of chromosomal aberration induction and its molecular mechanism needs further investigation.

结论守宫木具有一定诱发色体畸变遗传毒性。

In plants this is sometimes overcome by the doubling of the chromosome number, giving an allopolyploid.

在植中，这种不育现象有时可因为色体数目加倍而抵消，产生同源多倍体。

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体非整倍性可靠性。

Chromomere A small beadlike deeply staining structure seen in chromosomes during prophase of mitosis and meiosis.

在有丝分裂及减数分裂前期存在于色体上小念珠状着色深结构。

Chromosomes also determine the sex of animals.

染色体也决定动物性别。

Maple tree saccharorrhea sickness belongs to the euchromosome recessive hereditary disease.

枫糖尿症属于常染色体隐性遗传病。

The polytene chromosomes found in the salivary gland cells are among the largest chromosomes known today.

唾液腺细胞线染色体是目前已知最大染色体一。

The polymorphy of fronds and chromosome number of Ophioglossum petiolatum Hook.

有梗瓶尔小草叶性和染色体数目.

If both of a pair of homologous chromosomes are missing, nullisomy results.

如果一对同源染色体都缺失了，称为缺体。

Y chromosome has two types of polymorphism:metacentric (or submetacentric) and acrocentric chromosomes.

染色体有部(或亚部)和近端着丝粒染色体。

Lysogeny is a semi-permanent association between the phage and host chromosomes.

溶源性是噬菌体和寄生染色体间半永久联合。

This paper summarizes the roles of minichromosome maintenace proteins in DNA replication.

本文就微小染色体维持蛋白在复制作用简单综述。

About 1 in every 700 babies has this exbert cuppy, the extra copy.

每700个婴儿就有1个会有这余一条染色体。

Dynein also helps force apart chromosomes during cell division.

以及在细胞分裂，了机械能协助染色体分离。”

In the nucleoplasm chromosomes consisting of deoxyribonucleic acid (DNA) and proteins are present.

核质染色体由脱氧核糖核酸（DNA）和蛋白质构成。

A case of trisomy 22 liveborn female baby with multiple congenital anomalies is described.

摘要作者报告一例具有种先天性异常三染色体22症活产女婴。

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倍性现象。

Dentinogenesis imperfecta (DI) is a kind of mesodermal defect inherited in a simple autosomal dominant mode.

摘要牙本质成不良是一种体染色体显性遗传胚层缺陷。

Objective: Improve and optimize the method of Chromosome of zooblast.

改进和优化动物细胞染色体临时制片技术。

Methods :Using the chromo somal analysis and flurospectrop hotomytry methods to expel the chromosomal abnormality and mucoplysacch aridosis.

方法染色体检查排除染色体病,采用荧光光度计检测。

Conclusion Sauropus androgynus has certain genetic toxicity of chromosomal aberration induction and its molecular mechanism needs further investigation.

结论守宫木具有一定诱发染色体畸变遗传毒性。

In plants this is sometimes overcome by the doubling of the chromosome number, giving an allopolyploid.

在植物，这种不育现象有时可因为染色体数目加倍而抵消，产生同源倍体。

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可靠性。

Chromomere A small beadlike deeply staining structure seen in chromosomes during prophase of mitosis and meiosis.

在有丝分裂及减数分裂前期存在于染色体上小念珠状着色深结构。

Chromosomes also determine the sex of animals.

染色体也决定动物的性别。

Maple tree saccharorrhea sickness belongs to the euchromosome recessive hereditary disease.

枫糖尿症属于常染色体隐性遗传。

The polytene chromosomes found in the salivary gland cells are among the largest chromosomes known today.

腺细胞中的多线染色体是目前已知的最大染色体一。

The polymorphy of fronds and chromosome number of Ophioglossum petiolatum Hook.

有梗瓶尔小草叶的多形性和染色体数目.

If both of a pair of homologous chromosomes are missing, nullisomy results.

如果一对同源染色体都缺失了，称为缺体。

Y chromosome has two types of polymorphism:metacentric (or submetacentric) and acrocentric chromosomes.

染色体有中部(或亚中部)和近端着丝粒染色体。

Lysogeny is a semi-permanent association between the phage and host chromosomes.

溶源性是噬菌体和寄生染色体间的半永久联合。

This paper summarizes the roles of minichromosome maintenace proteins in DNA replication.

本文就微小染色体维持蛋白在复制中的作用简单综述。

About 1 in every 700 babies has this exbert cuppy, the extra copy.

每700个婴儿中就有1个会有这多余的一条染色体。

Dynein also helps force apart chromosomes during cell division.

以及在细胞分裂中，提供了机械能协助染色体的分离。”

In the nucleoplasm chromosomes consisting of deoxyribonucleic acid (DNA) and proteins are present.

核质中的染色体由脱氧核糖核酸（DNA）和蛋白质。

A case of trisomy 22 liveborn female baby with multiple congenital anomalies is described.

要作者报告一例具有多种先天性异常的三染色体22症的活产女婴。

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的多倍性现象。

Dentinogenesis imperfecta (DI) is a kind of mesodermal defect inherited in a simple autosomal dominant mode.

要牙本质形不良是一种体染色体显性遗传的中胚层缺陷。

Objective: Improve and optimize the method of Chromosome of zooblast.

改进和优化动物细胞染色体的临时制片技术。

Methods :Using the chromo somal analysis and flurospectrop hotomytry methods to expel the chromosomal abnormality and mucoplysacch aridosis.

方法染色体检查排除染色体,采用荧光光度计检测。

Conclusion Sauropus androgynus has certain genetic toxicity of chromosomal aberration induction and its molecular mechanism needs further investigation.

结论守宫木具有一定的诱发染色体畸变的遗传毒性。

In plants this is sometimes overcome by the doubling of the chromosome number, giving an allopolyploid.

在植物中，这种不育现象有时可因为染色体数目加倍而抵消，产生同源多倍体。

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可靠性。

Chromomere A small beadlike deeply staining structure seen in chromosomes during prophase of mitosis and meiosis.

在有丝分裂及减数分裂的前期存在于染色体上的小念珠状的着色深的结。