If the Y chromosome is detected, the fetus is male.
如果检测到Y染色体，则胎儿是个男性。
Objective: To investigate the possible clinical effects of long Y chromosome.
目的探讨大y染色体核型是否能造成临床效应。
Objective: to probe into clinical significance of long or short Y chromosome.
目的探讨大小y染色体核型的临床意义。
The Y chromosome makes its owner male because it carries the male-determining gene.
Y染色体让携带者之所以成为男性，是因为它携带了雄性决定基因。
To establish the rate of mutation, the team examined an area of the Y chromosome.
为了确定基因突变的速率，这个团队对他们Y染色体的某个区域进行了仔细的测定。
The gender ratio of X chromosome and Y chromosome was almost same in the haploid.
单倍体中含有X-性染色体和含有Y-性染色体的性比基本相同。
Objective To discuss the clinical significance of long Y chromosome configuration.
目的探讨大y染色体核型的临床意义。
New, still unpublished work reveals that the Neandertal Y chromosome differs from the human one.
尚未发表的新近研究显示，尼安·德塔人的Y染色体与人类不同。
The X chromosome is three times the size of the Y chromosome and carries 100 times the genetic information.
人体X染色体的显微扫描照片。 （得到照片研究中心允许而复制） X染色体是Y染色体的三倍大，而且也传递着比其多100倍的基因信息。
The major portion of the Y chromosome, the male specific region, is inherited intact from fathers to sons.
Y染色体的大部分，男性特有的区域，是从父到子原封不动地遗传的。
Objective To study the diagnosis of ZFY gene on human Y chromosome and its application in tissue engineering.
目的探讨人的Y染色体ZFY基因诊断在组织工程中的应用。
The main contents are as follows:Chapter one mainly introduces the whole characteristics of human Y chromosome;
第一章主要介绍人类Y染色体的整体特征；
We anticipate that certain forms of the Y chromosome will be more common in those with AAA than across the general population.
我们预期在AAA患者中y染色体的某些形式比一般人群更为常见。
Objective:To explore the relationship between Y chromosome microdeletion and non-idiopathic infertility in male cases with dyszoospermia.
目的：探讨非特发性男性不育症与Y染色体微缺失的关系。
Abstract: Objective To explore the identification method of full sibling between two males with microdeletion and mutation of Y chromosome.
摘要目的探讨y染色体微缺失和突变时，两男性个体间的全同胞关系鉴定。
Y chromosome is another focus of human evolutionary studies after mitochondrial DNA, which has also approved the "out of Africa" hypothesis.
染色体是继线粒体之后的研究人类进化的又一热点，通过对其上的多态性位点研究也证实了非洲起源说。
The analysis of correlation between karyotype and AZF microdeletion on Y chromosome for patients with azoospermia and severe oligozoospermia.
目的：研究男性原发性无精及严重少精症患者Y染色体AZF微缺失区域与临床表型的关系。
Women do not have a Y chromosome, so they cannot be tested in the same way, although millions are likely also to be descended from the warlord.
女性没有Y染色体，因此，她们不能通过相同的检测方法来查找祖先，虽然可能很多女性也是成吉思汗的后代。
Results: some genes including several genes on Y chromosome and androgen receptor gene were demonstrated to be associated with spermatogenesis impairment.
结果：Y染色体上的一些基因、雄性激素受体基因等被证实与生精障碍相关。
It's possible scientists could have looked at genetic similarities in the mitochondria or even Y chromosome of samples as well, depending on what's available to test.
有可能，科学家依据哪个能够用来进行测试，可以看到样本中线粒体或Y染色体的遗传相似性。
In much of the world they still enjoy social and legal privileges simply because they have a Y chromosome. So it might seem odd to worry about the plight of men.
在大多数国家里男人仅仅因为拥有一条Y染色体便享有在社会和法律上的特权，这样看来，担心男性的“悲催命运”般的困境似乎是在杞人忧天。
“Natural selection is shaping the Y and keeping it vital to a degree that is really at odds with the idea of the last 50 years of a rotting Y chromosome, ” Dr. Page said.
佩奇博士说：“自然选择塑造了Y染色体，50年来，我们为Y染色体的退化争论不休，自然选择论更是加剧了这种争论。
The syndrome may be the result of Y chromosome recombination gone awry, Page speculates, when the chromosome inadvertently becomes a palindrome with no gap in the center.
Page推测，这个综合症可能是由于Y染色体重组时出错，导致染色体中不小心出现了一段中心没有空隙的回文。
Professor Robinson's Y chromosome is an exact match for eight of the nine markers, and one mutation is expected over the 800 years that separate him from the Mongol ruler.
他的一个基因变异被认为已经有800年的历史了，也就是说，他的基因从800年前与成吉思汗分离。
There were 17 cases of chromosome polymorphism, accounting for 9.83% of all abnormal karyotypes. It contains Y chromosome, secondary constriction, and variation of satellites.
染色体多态性17例，占异常核型的9.83%，主要包括Y染色体多态性、次缢痕和随体的变异。
Male infertility can be induced by many factors, and extensive studies have strongly indicated that Y chromosome microdeletions are closely related to male reproductive dysfunction.
男性不育原因多样，大量研究表明Y染色体微缺失与男性不育的关系密切。
The results suggest that the Y chromosome heterochromatin appears to have a modifying effect on the phenotypic relationship between morphophysiological traits during human ontogenesis.
结果表明，Y染色体异染色质可能在人的个体发育过程中对形态生理学性状间的表型关系起一种修饰作用。
The team sequenced the same piece of DNA - 10,000,000 or so letters or 'nucleotides' from the Y chromosome - from two men separated by 13 generations, and counted the number of differences.
这个小组以相隔了13代的两个男性为测试对象，在其Y染色体相同区域上选取长约10， 000， 000核苷酸片段进行了测序，并计算了两者之间的差异。
The team sequenced the same piece of DNA - 10,000,000 or so letters or 'nucleotides' from the Y chromosome - from two men separated by 13 generations, and counted the number of differences.
这个小组以相隔了13代的两个男性为测试对象，在其Y染色体相同区域上选取长约10， 000， 000核苷酸片段进行了测序，并计算了两者之间的差异。
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