X chromosome

The attenuated phenotype should be owing to skewed X inactivation derivative X chromosome.

部分1-三体的表型弱化可能与X染色体偏颇失活有关.

Numerical Ranges of Normal Dual Mapping The X chromosome was normal.

正规对偶映象的数值域X染色体无变化。

Rapid detectin of chromosome rearrangement in medical diagnostic X-ray workers by using fluorescence in situ gybridization and Study on dose estimation.

用荧光原位杂交快速检测医用诊断x射线工作者染色体结构重排及其剂量估算的探讨。

X chromosome centromeric alpha satellite DNA variation in Klinefelter's syndrome patients and their parents

Klinefelter综合征及双亲X染色体着丝粒区α-卫星DNA变异研究

The X chromosome is metacentric, the Y chromosome being telocentric.

x染色体为中部着丝点，y染色体为端部着丝点。

An X chromosome combines with the mother's X chromosome to make a baby girl ( XX) and a Y chromosome will combine with the mother's to make a boy ( XY).

X染色体与母亲的X染色体结合，就会生出女孩（XX）；而Y染色体和母亲的X染色体结合则会生出男孩（XY）。

The whole X chromosome were dyed light.

X染色体不出现C带阳性区，整个被浅染；

Biodosimetry for medical diagnostic X-ray workers using stable chromosome aberration

用稳定性染色体畸变作为医用诊断X射线工作者生物剂量估算的研究

Non-random XCI was not the main XCI pattern in RTT patients. The priority inactive X chromosome was mainly of paternal origin.

RTT患儿非随机失活的X染色体主要起源于父亲。

One-hundred-forty-four human X chromosome genes had no counterparts in mice.

人类X染色体上有144组基因不同于老鼠。

The abnormality and genetic disorders of X chromosome involved in premature ovarian failure

X染色体异常及其基因缺陷在卵巢早衰发病机制中的研究

Method The fluorescence signal of samples from 35 cases in different periods after sex-mismatched allo-HSCT were detected by interphase FISH using chromosome enumeration probes ( CEP) X and Y.

方法采用X、Y染色体探针和间期双色间期FISH法检测35例异性异基因造血干细胞移植受者移植后不同时期的性染色体荧光杂交信号。并设对照组，分析检测的有效率。

The use of the X chromosome in population genetics is still in its infancy.

对X染色体的使用在群体遗传学中仍处于初级阶段.

Sometimes there may be abnormalities in the X chromosome in only some cells in the body.

有时可能会有异常的X染色体中，只有一些细胞在人体内。

Concerning characteristics that are determined by genes carried on the sex chromosomes ( on the X chromosome in particular).

关于携带性染色体（尤指x染色体）基因决定的特征。

A study of the abnormal X chromosome in schizophrenic patients

精神分裂症患者X染色体异常的研究

Women with the syndrome are missing one or part of their second X chromosome.

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。

Chicken PGCs from a line of White Leghorns were microinjected into Maya duck blastoderms at stage ⅹ. Extragonadal development of donor PGCs in chicken duck chimeric embryos were studied by in situ hybridization with W chromosome specific DNA probes.

通过微注射法将鸡原始生殖细胞（PGCs）注入到鸭的胚盘下腔中，用鸡W染色体DNA探针通过原位杂交的方法对供体PGCs在嵌合体胚胎性腺外的发育作了研究。

54.5% of these cases involve the structural rearrangement of X chromosome.

其中6例（54.5%）涉及X染色体结构异常。

Methods Firstly, X chromosome scanning was used to exclude X chromosome.

方法先进行X染色体扫查，排除致病基因位于X染色体的可能；

The X chromosome was normal. PCR amplification;

X染色体无变化。普通PCR扩增目的片段；

The X chromosome is therefore the logical place to turn for more information.

因此X染色体也就合乎逻辑的成为了更多信息的来源.

It is nomal in scope. The X chromosome was normal.

属正常范围。X染色体无变化。

As MeCP 2 resides on the X-chromosome, this meant studying male mice as females have two X-chromosomes.

由于MeCP2位于 X 染色体上, 所以他们选择研究雄性老鼠,因为雌性老鼠含有两个 X 染色体.

Is Photosensitive Epilepsy Less Common in Males Due to Variation in X Chromosome Photopigment Genes?

光敏感性癫痫在男性较少见是否由于X染色头感光色素基因变异?

How can an X chromosome be nearly as big as the head of the sperm cell?

染色体怎么会接近性子头部的大小?

Proceeding of research on X chromosome genetic markers

X染色体遗传标记研究进展

Study of fragile X chromosome in the child patients with inherent mental retardation

先天智力低下患儿脆性X染色体分析

Fewer than 1 % of females affected because the trait is carried on the X chromosome.

不到1%的女性受到影响,因为这种特性是与X染色体上.

The x-chromosome has many genes for which there are no paired genes on the Y-chromosome.

x染色体有许多在Y染色体上不能配对的基因。