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

摘要运用核系数聚类分析方法,分析了蚧属7种的亲缘关系与系统演化。

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agalite, agalloch, agallochum, Agallol, agalma, agalmatolite, agalorrhea, agalwood, agama, agamae,

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3G, 401(K), a,

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Osmosis-

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裂过程中的某个时刻,结果是形成另一个马赛克核型。

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Osmosis-

There are three potential karyotype scenarios associated with Turner syndrome.

与特纳综合征相关的潜在核型有三种。

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Osmosis-生殖

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,可进行染核型析。

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Osmosis-

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核型是X染只有部缺失。

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Osmosis-

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

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

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Osmosis-生殖

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

最可能的核型是45,X,意味着这个人有45条染,只有一条X染

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Osmosis-

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

核型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

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,意味着其染核型为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

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

您是否进行过核型测试以确定您的染?对你所有激素水平的全血检测怎么样?

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Osmosis-

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核型,而另一些细胞具有46,XX核型。

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Osmosis-生殖

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,超声检测以及染核型析也被用于识别潜在病因。

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Osmosis-内

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,可进行核型析以寻找染异常,如果有脆性X染综合征家族史,可以进行特定的基因检测。

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Osmosis-

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染核型细胞的比例。

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agamogenesis, agamogenetic, agamont, agamospecies, agamospermy, agamous, agamy, Agana, aganglionic, Aganippe,

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3G, 401(K), a,
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