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- XXY性染色體改變XXY sex chromosome alteration
- 目的檢測中國兒童孤獨癥患者的特征性染色體改變。Objective To detect the characteristic chromosomal changes in Chinese children with infantile autism.
- X0性染色體改變X0 sex chromosome alteration
- XYY性染色體改變XYY sex chromosome alteration
- 一種罕見(jiàn)X染色體改變與X連鎖綜合征型耳聾的關(guān)系Infrequent X chromosome abnormality and X-linked syndromic deafness
- XXY三體性XXY trisomy
- 知性intellectuality
- 染色體chromosome
- 69,XXY伴嚴重生長(cháng)遲緩及眼球突出病例的產(chǎn)前診斷Prediagnosis a case of 69, XXY with severe asymmetrical fetal growth and eyeballs standout abnormally
- 耐久性wear
- XXY染色體綜合征XXY syndrome
- 雙性戀bisexual love
- 保障性indemnificatory
- 有性sexual
- 敏感性sensibility
- 常染色體autosome
- 整體性globality
- 魯棒性robustness
- 災難性的disastrous
- 其次為大Y染色體4 例,檢出率為7.02%,占異常核型的7.39%。 46,XY/47,XXY和47,XYY各1例,檢出率為1.75%,占異常核型的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.
