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1.The cluster analysis method of karyotype resemblance-near coefficient was used to study the relationship and evolution of seven species in the genus Kerria.

1.摘要运用核型近似系数聚类法,胶蚧属7种紫胶虫的亲缘关系与系统演化。

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gemmulation, gemmule, gemmuliferous, gemmulostasin, gemmy, gemnivirus, gemnology, Gemolite, gemological, gemologist,

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3G, 401(K), a,

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Osmosis-遗传

1.This can also happen at some point during mitosis, and the result is another mosaic karyotype.

这种情况也可能发生在有丝裂过程中的某个时刻,结果是形成另一个马赛克

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Osmosis-遗传

2.There are three potential karyotype scenarios associated with Turner syndrome.

与特纳综合征相关的潜在有三种。

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Osmosis-生殖

3.A karyotype can be done for Turner syndrome and androgen insensitivity syndrome.

对于Turner综合征、雄激素敏感综合征,可进行染色析。

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Osmosis-遗传

4.The least common karyotype in Turner syndrome is where there's only a part of the X chromosome missing.

特纳综合征中最常见的是X染色只有失。

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Osmosis-遗传

5.Klinefelter syndrome is diagnosed with a karyotype which visualizes each chromosome including the X, Y, and extra X chromosomes.

析可观察到患者的每条染色,包括X、Y与额外的X染色,可用来确诊Klinefelter综合征。

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Osmosis-生殖

6.The most common karyotype is 45, X, which means the person has 45 chromosomes, of which only one is an X chromosome.

最可能的是45,X,意味着这个人有45条染色,只有一条X染色

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Osmosis-遗传

7.A karyotype can be done before birth with an amniocentesis or at any time after birth with the blood test.

析在出生前就可以用羊膜穿刺术取样或在出生后采血取样。

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Osmosis-生殖

8.In this case, the individual is biologically male, which means they have a 46, XY karyotype, but their androgen receptors don't respond to testosterone.

这种情况下,患者生物学性别为男性,意味着其染色为46,XY,但他们的雄激素受能对睾酮做出反应。

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TED演讲(音频版) 2019年2月合集

9.Have you had a karyotype test to determine your chromosomes? What about a full blood panel for all of your hormone levels?

您是否进行过测试以确定您的染色?对你所有激素水平的全血检测怎么样?机翻

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Osmosis-遗传

10.The next most common scenario is mosaicism, meaning the individuals have some cells in their body with the 45, X karyotype and others with a 46, XX karyotype.

另一种最常见的情况是嵌合,这意味着个内的一些细胞具有45,X,而另一些细胞具有46,XX

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Osmosis-生殖

11.Other associated symptoms, serum FSH, LH, estrogen and testosterone, as well as an ultrasound or a karyotype can be used to identify the underlying condition.

其它伴随症状,检测血清FSH、LH、雌激素和睾酮水平,超声检测以及染色析也被用于识别潜在病因。

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Osmosis-内

12.Additionally, a karyotype can be done to look for chromosomal abnormalities and specific genetic tests can be ordered if there's a family history of Fragile-X syndrome.

此外,可进行析以寻找染色异常,如果有脆性X染色综合征家族史,可以进行特定的基因检测。

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Osmosis-遗传

13.Just how many of these abnormalities linked with Turner syndrome are actually present depends on the proportion of cells the person has with the 45, X karyotype.

这些与特纳综合征相关的异常会出现多少,取决于一个人拥有45,X染色细胞的比例。

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gender-bender, genderist, genders, gending, gene, gene expression, gene mutation, geneal., genealogical, genealogist,

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3G, 401(K), a,
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