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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.
