x chromosome

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

湖南土家族群體X染色體10個STR位點的遺傳多態性及法醫學應用價值評估

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

藏族X染色體10個STR位點的遺傳多態性

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

X染色體上六個短串聯重復序列基因座遺傳多態性研究

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

3個X染色體短串聯重復的復合擴增及其多態性

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

目的以無關個體為研究對象,研究鄂溫克族人群X染色體5個STR位點的遺傳多態性,建立群體遺傳數據庫。

The methylation modification accompanying X chromosome inactivation;

伴隨X染色體失活的甲基化修飾

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

多點微切割的病變中,10例呈現不同的X染色體失活類型。

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

目的探討X-連鎖遲發性脊椎骨骺發育不良(SEDL)基因逃避X染色體失活(XCI)及與臨床表型的關系。

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)是人類常見的X染色體連鎖隱性遺傳的神經-肌肉系統疾病,發病率高,至今尚無有效的治療方法。