核型分析结果显示，ZP - 1细胞为正常女性染色体结构。
Karyotype analysis showed that ZP-1 cells have a normal female chromosome structure.
在这八周了，这些染色体是男性胚胎和女性胚胎的唯一区别。
For a few weeks, these chromosomes are all that differentiates male embryos from female embryos.
科学家认为，女性更健康的原因可能在于微rna(核糖核酸)，它是染色体上RNA编码的短片段。
The reason why women are more robust appears to be microRNAs - short strands of RNA encoded on the chromosome, scientists believe.
高达一半以上年轻女性（39岁以后则高达75%）的卵细胞有异常染色体。
Up to half the eggs of younger women, and up to 75% in women over 39, have abnormal chromosomes.
这使只有一条X染色体的男性处于不利地位，而女性拥有两条，所以即使一条上的免疫基因不能发挥作用，另一条上的也能起到弥补作用。
This leaves men at a disadvantage since they only have one X chromosome. Women have two, so that even when immunity genes are silenced on one the other can compensate.
现在猜测这些疾病基因可能在X染色体上面，这意味着女性有着第二条基因去抵消的优势。
Now some of these [disease genes] may be on the X chromosome, [meaning that women who have the second X chromosome with which to compensate, would have an advantage].
有一种罕见的疾病叫作“特纳氏综合症”(Turner ' s Syndrome)。患有这种疾病的女性，性别基因(XX)缺失了一条染色体x，所以也被称为XO女孩。
There is a rare condition known as Turner's Syndrome where a genetic female (XX) is missing one of the X chromosomes and she is known as an XO girl.
患有特纳综合症的女性往往缺失一种或部分第二X染色体。
Women with the syndrome are missing one or part of their second X chromosome.
染色体嵌合现象并不是男性与女性之间唯一的基因差别。
X chromosome mosaicism is not the only genetic difference between males and females.
特纳综合症通常由染色体的问题所导致，这种疾病会让女性无法生殖且身高比常人矮。
Turner Syndrome usually results from a problem with the chromosomes and can leave women infertile and shorter than normal.
目的探讨女性年龄对卵母细胞纺锤体和染色体构型的影响。
Objective To study the effect of maternal age on meiotic spindle and chromosome configuration of oocytes.
这是用来分析染色体组成的女性。
This is used to analyse the chromosomal composition of the female.
女性作为X染色体的杂合子在人类的健康与疾病中及重要作用，并可避免X连锁遗产性疾病在女性中发生。
Female mosaicism of the X chromosome has major implications for human health and disease and is the leading cause of female protection from X-linked genetic disorders.
本文报道了一例两条9号染色体次缢痕缺失的女性病例，临床表现为严重智力低下和语言障碍。
This report describes a female ease who is complete deletion of secondary constriction on two chromosomes 9. The major clinical phenomenon is severe mental retardation.
本实验将通过研究女性肾透明细胞癌及正常肾组织的X染色体失活类型判断肾透明细胞癌克隆起源。
To assess the clonal origin of renal clear cell carcinomas by the study of X-chromosome inactivation pattern in female clear cell renal carcinomas and normal renal tissues.
方法应用原位引物标记(PRINS)在8例女性外周血淋巴细胞培养标本中检测了X、18号染色体。
Methods Chromosomes X, 18 were detected by the primed in situ labeling (PRINS) in eight samples of female peripheral blood cultures.
结论：染色体核型为45,xo个体大部分分化为女性，但少数可能向男性分化。
Conclusion: Most individuals with chromosome karyotype 45, XO can differentiate to female, but a few can differentiate to male.
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。
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.
但是它只能检测胚胎内不到一半的染色体，因此PGD对预测整个胚胎的健康情况并不理想，而且它对于大多数女性而言并不实用。
But it tests fewer than half of the chromosomes in an embryo, so it's not a perfect indicator of overall embryo health and it hasn't been all that useful for most women.
另外，女性还有两条X染色体，而男性则还有一条X染色体和一条Y染色体。
Also, females have two "X chromosomes." males have one "X" and one "Y" chromosome.
男人也拥有女性的X染色体拥有线索女性祖先的路线，可以判断第一海盗入侵者带来了他们的家庭或与他们来的。
Men also possess a female X chromosome that holds clues about the female ancestral line and could tell whether the first Viking invaders brought their families with them or came alone.
男人也拥有女性的X染色体拥有线索女性祖先的路线，可以判断第一海盗入侵者带来了他们的家庭或与他们来的。
Men also possess a female X chromosome that holds clues about the female ancestral line and could tell whether the first Viking invaders brought their families with them or came alone.
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