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。