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(tài)性及法醫(yī)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(tài)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(lián)重復序列基因座遺傳多態(tài)性研究

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

3個X染色體短串聯(lián)重復的復合擴增及其多態(tài)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(tài)性,建立群體遺傳數(shù)據(jù)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(xiàn)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(fā)性脊椎骨骺發(fā)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(jīng)-肌肉系統(tǒng)疾病,發(fā)病率高,至今尚無有效的治療方法。