![X chromosome](../cache/558058.jpg)
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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。
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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。
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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)。
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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
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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。
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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。
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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。
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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;
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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
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Proceeding of research on X chromosome genetic markers
X染色体遗传标记研究进展
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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。
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The X chromosome was normal . PCR amplification ;
X染色体无变化。普通PCR扩增目的片段;
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The whole X chromosome were dyed light .
X染色体不出现C带阳性区,整个被浅染;
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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
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It is nomal in scope . The X chromosome was normal .
属正常范围。X染色体无变化。
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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。
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Clearly , the X chromosome Xceeds its feminine responsibilities .
很明显,X染色体不光对雌性起作用。
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A Family of Fragile Site X Chromosome
一个脆性位点X的家庭
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meeting that X chromosome of the egg .
遇到携带着X染色体的卵子
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The X chromosome was normal .
X染色体无变化。
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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
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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
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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。
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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
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X Chromosome Inactivation in Mammalian PRION , LIFE AND PATHOGEN
哺乳动物X染色体失活机制
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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
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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。
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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。
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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。
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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