Mechanisms of the sex chromosome aberration causing abnomal sex development were discussed.

1、

Among them, there were 9 cases of abnormal chromosomal number, 4 cases of abnormal structure aberration and 2 cases of number anomalies of sex chromosome.

其中常染色体数目异常9例，结构异常4例，性染色体数目异常2例。

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2、

The No. 5 is sex chromosome ( ZW type).

5为异型性染色体（ZW型）；

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3、

Conclusion Sex chromosome aberration is the most important cause that results in sex differential distortion.

结论性染色体异常是导致性分化异常的重要原因之一。

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4、

The sex chromosome is XY.

性染色体为XY。

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5、

Non-gonadal defect and abnormal sex chromosome syndrome

无性腺缺陷－性染色体异常综合征

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6、

Sex chromosome abnormalities and analysis of the relationship between male infertility

性染色体异常与男性不育的关系分析

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7、

Similar to Mark W. The sex chromosome.

采用类似于Mark W.性染色体Z为中着丝粒染色体，W为近端着丝粒染色体。

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8、

Chromosome Diseases of Human ⅱ. Sex Chromosome Diseases

人类染色体疾病

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9、

Among 19 cases autosomal abnormal are 14 cases, sex chromosome abnormal are 5 cases.

其中，常染色体异常14例，性染色体异常5例。

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10、

Unlike other sex chromosome aneuploidy, there are no general characteristic physical features for triple X patients.

与其他性染色体非整倍体不同，XXX核型的患者并没有显著的身体特征。

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11、

Study on the Breeding of Male Silkworm Varieties Using Lethal Lines Balanced on Silkworm Sex Chromosome

利用性连锁平衡致死系进行雄蚕品种选育的方法研究

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12、

Conclusion: Turner's syndrome is the most common abnormality of sex chromosome in children.

结论：Turner氏综合征是儿童性染色体异常中最常见的类型。

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13、

Objective: To investigate abnormality of sex chromosome in children and its prenatal diagnosis.

目的：研究儿童性染色体异常及产前诊断性染色体异常。

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14、

Combined with ultrasonic examination in perinatal stage, karyotype analysis and FISH can help to screen those chidren with abnormal sex chromosome.

应用染色体核型分析和荧光原位杂交技术，同时结合围产期超声检查进行产前诊断，可筛选性染色体异常患儿。

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15、

There were 61 cases of sex chromosome abnormality accounting for 37.20% in the chromosomal abnormal karyotype;

性染色体异常61例，占染色体异常核型的37.20%；

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16、

Conclusion The sex chromosome abnormality is one of the major causes of primary azoospermia.

结论性染色体异常是原发性无精子症发生的根本原因之一。

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17、

Sperm sex chromosome analysis and preimplantation genetic diagnosis of patients with sex chromosome anomalies

外周血性染色体异常患者精子染色体分析及植入前遗传学诊断

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18、

Objective To explore the clinical and biological characteristics of 12 cases of t ( 8; 21) acute myeloid leukemia with sex chromosome loss.

目的探讨12例伴有性染色体丢失的t（8；21）急性髓系白血病患者的临床和生物学特征。

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19、

Y chromosome is sex chromosome, it can only be passed to all maleness.

Y染色体为性染色体，呈全男性遗传。

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20、

Diagnosis of sex chromosome aberration using fluorescence in suit hybridization

荧光原位杂交技术诊断性染色体畸变的应用

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