X chromosome

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。

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）。

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

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。

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。

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。

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；

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

Proceeding of research on X chromosome genetic markers

X染色体遗传标记研究进展

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。

The X chromosome was normal . PCR amplification ;

X染色体无变化。普通PCR扩增目的片段；

The whole X chromosome were dyed light .

X染色体不出现C带阳性区，整个被浅染；

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

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

属正常范围。X染色体无变化。

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。

Clearly , the X chromosome Xceeds its feminine responsibilities .

很明显，X染色体不光对雌性起作用。

A Family of Fragile Site X Chromosome

一个脆性位点X的家庭

meeting that X chromosome of the egg .

遇到携带着X染色体的卵子

The X chromosome was normal .

X染色体无变化。

Development and Application of 4 X Chromosome STR Loci Markers Typing System for Forensic Genetics

四个X-STR基因座荧光复合扩增体系的建立及其法医遗传学研究

RFLPs Study of Parental Origin and Mechanism of 3 Cases with X Chromosome Structural Abnormality

RFLPs研究三例X染色体结构异常的起源和形成机理

As with mice , the TEX11 gene is also located on the human X chromosome .

同小鼠一样，人体内的TEX11基因也位于X染色体上。

Genetic polymorphism of X chromosome short tandem repeats locus

X染色体短串联重复序列基因座的遗传多态性

X Chromosome Inactivation in Mammalian PRION , LIFE AND PATHOGEN

哺乳动物X染色体失活机制

Skewed X Chromosome Inactivation and Imprinted / X-linked Gene Expression in Human Embryonic Stem Cells

人类胚胎干细胞X染色体倾斜性失活及印迹、X连锁基因表达状态

This report summarized the proceeding of research on X chromosome genetic markers in the clinical and forensic context .

本文收集了国内外X染色体遗传标记在临床疾病诊断及法医DNA工作者实践中的研究和应用资料，汇总报道了X染色体遗传标记的研究进展。

X chromosome mosaicism is not the only genetic difference between males and females .

染色体嵌合现象并不是男性与女性之间唯一的基因差别。

The chromosome carrying the male determining genes is designated Y and the corresponding female one the X chromosome .

携带决定男性的基因的染色体称为Y染色体，携带决定女性的基因的染色体称为X染色体。

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