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- XXY性染色体改变 XXY sex chromosome alteration
- 目的检测中国儿童孤独症患者的特征性染色体改变。 Objective To detect the characteristic chromosomal changes in Chinese children with infantile autism.
- X0性染色体改变 X0 sex chromosome alteration
- XYY性染色体改变 XYY sex chromosome alteration
- 一种罕见X染色体改变与X连锁综合征型耳聋的关系 Infrequent X chromosome abnormality and X-linked syndromic deafness
- XXY三体性 XXY trisomy
- 知性 intellectuality
- 染色体 chromosome
- 69,XXY伴严重生长迟缓及眼球突出病例的产前诊断 Prediagnosis a case of 69, XXY with severe asymmetrical fetal growth and eyeballs standout abnormally
- 耐久性 wear
- XXY染色体综合征 XXY syndrome
- 双性恋 bisexual love
- 保障性 indemnificatory
- 有性 sexual
- 敏感性 sensibility
- 常染色体 autosome
- 整体性 globality
- 鲁棒性 robustness
- 灾难性的 disastrous
- 其次为大Y染色体4 例,检出率为7.02%,占异常核型的7.39%。 46,XY/47,XXY和47,XYY各1例,检出率为1.75%,占异常核型的4.35%。 then were big Y chromosome, four cases, accounting for 7.02%25 of patients studied and 17.39%25 of those with ACK: 46,XY/47,XXY and 47,XXY, one case for each type.
