Chromosomes also determine the sex of animals.
染决定动物的性别。
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目前已知的最大染之一。
The polymorphy of fronds and chromosome number of Ophioglossum petiolatum Hook.
有梗瓶尔小草叶的多形性和染数目.
If both of a pair of homologous chromosomes are missing, nullisomy results.
如果一对同源染都缺失了，称为缺。
Y chromosome has two types of polymorphism:metacentric (or submetacentric) and acrocentric chromosomes.
染有中部(或亚中部)和近端着丝粒染。
Lysogeny is a semi-permanent association between the phage and host chromosomes.
溶源性噬菌和寄生染之间的半永久联合。
This paper summarizes the roles of minichromosome maintenace proteins in DNA replication.
本文就微小染维持蛋白在复制中的用简单综述。
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。
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的分离。”
In the nucleoplasm chromosomes consisting of deoxyribonucleic acid (DNA) and proteins are present.
核质中的染由脱氧核糖核酸（DNA）和蛋白质构成。
A case of trisomy 22 liveborn female baby with multiple congenital anomalies is described.
摘要告一例具有多种先天性异常的三染22症的活产女婴。
Autopolyploidy A type of polyploidy involving the multiplication of chromo-some sets from only one species.
通常由同一个，同一纯种的染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一种染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.
方法染检查排除染病,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上的小念珠状的着深的结构。
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In the translocation, the two chromosomes swap large pieces of chromosome with each other.
在易位过程中，两条染色交换了大量的染色片段。
Now males males have one X and one Y chromosome, and females have two X chromosomes.
那么，男有一个X染色和一个Y染色，有两个X染色。
The genetic problem is linked to the X sex chromosome.
基因疾病与X染色有关。
One known mechanism for how a follicular lymphoma develops, is a chromosomal translocation between chromosome 14 and chromosome 18.
一种的滤泡淋巴瘤发生机制，是14号染色和18号染色之间的染色易位。
Those are the structures in our cells that contain DNA.
染色是细胞中含有 DNA 的结构。
Men inherit their Y chromosomes from their fathers.
男从父亲那里继承Y染色。
In fact, it has a big role in making sperm.
X染色在精子的形成过程中起重要作用。
We know that radiation causes or will induce these chromosome aberrations, or rearrangement of the chromosomes.
我辐射会引起或诱发染色的畸变或重排。
That's because the gene that's responsible for making G6PD is on the X chromosome.
这是因为X染色基因决定G6PD。
Down Syndrome is a disorder of the chromosomes.
唐氏综合症是染色疾病。
The other two were genes that help maintain the structure of chromosomes.
其他两个是帮助维护持染色结构的基因。
In some cases, it's linked to chromosomal abnormalities like Turner syndrome, where an X chromosome is missing.
在某些情况下，它与染色异常有关，如Turner综合征，其X染色缺失。
All cells contain two sets of chromosomes.
所有的细胞都含有两套染色。
Most people have 20 chromosomes, but the presence of an extra 21st chromosome creates the disorder.
绝大多数人拥有20对染色，然而多出的另一对染色会导致该疾病的产生。
HeLa cells themselves actually have around 80 highly mutated chromosomes.
海拉细胞自己拥有大约八十条高度变异的染色。
The primary oocyte has 46 chromosomes, but eventually it has to turn into a gamete with only 23 chromosomes.
初级卵母细胞有46条染色，但是最终会变成只有23条染色的配子。
We all have XX chromosomes, right?
我都有XX染色，对吧？
Dr Jacquemont's study, however, found only a limited role for X-chromosome mutations.
然而Jacquemont医生的研究发现X染色突变的作用有限。
For one, there were signs of radiation damage in Scott's chromosomes.
首先，斯科特的染色中有辐射损伤的痕迹。
Alleles are the parts of a chromosome that encode specific genetic traits.
等位基因是染色上编码特定遗传特征的部分。
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划词翻译
详细解释
决定动物的性别。
目前已知的最大
用简单综述。
告一例具有多种先天性异常的三
有一个X
的滤泡
