x chromosome

Genetic polymorphisms of ten X chromosome STR loci in Hunan Tujia population and their forensic evaluation;

湖南土家族群体X染色体10个STR位点的遗传多态性及法医学应用价值评估

Genetic polymorphisms of 10 X chromosome STR loci in a Chinese Tibetan population;

藏族X染色体10个STR位点的遗传多态性

Genetic polymorphism of six short tandem repeat loci on the X chromosome in a Han race population in China;

X染色体上六个短串联重复序列基因座遗传多态性研究

Polymorphism and multiplex amplification of 3 X-chromosomespecific short tandem repeat loci;

3个X染色体短串联重复的复合扩增及其多态性

Genetic Polymorphism of DXS7423,DXS7424,DXS7132,DXS7133,DXS6804 Loci on X-chromosomein Ewenke Population;

目的以无关个体为研究对象,研究鄂温克族人群X染色体5个STR位点的遗传多态性,建立群体遗传数据库。

The methylation modification accompanying X chromosome inactivation;

伴随X染色体失活的甲基化修饰

Methods X chromosome inactivation pattern was assessed in 22 cases of cervical SCC and 48 cases CIN.

多点微切割的病变中,10例呈现不同的X染色体失活类型。

Objective To explore the relationship between X - linked spondyloepiphyseal dysplasia tarda (SEDL) gene escaping X chromosome inactivation( XCI) and SEDL phenotype.

目的探讨X-连锁迟发性脊椎骨骺发育不良(SEDL)基因逃避X染色体失活(XCI)及与临床表型的关系。

The Duchenne and Becker muscular dystrophies(DMD/BMD) are X-linked recessive diseases of the neuromuscular system,which are characterized by high morbility.

Duchenne/Beckermuscu lar dystroph ies(DMD/BMD)是人类常见的X染色体连锁隐性遗传的神经-肌肉系统疾病,发病率高,至今尚无有效的治疗方法。