sex chromosome

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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A Study of Sex Chromosome in Carassius auratus by BrdU-Hoechst 33258-Giemsa Technique

应用BrdU-Hoechst33258-Giemsa技术对鲫鱼性染色体的研究

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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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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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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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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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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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Among these karyotype, 263 cases were euchromosome malformation, 194 were sex chromosome malformation.

染色体异常中常染色体异常263例，性染色体异常194例；

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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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Research Progress on Sex Chromosome Evolution in Dioecious Plants

雌雄异株植物性染色体演化研究进展

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The sex chromosome is XY.

性染色体为XY。

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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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Rapid detection of numerical sex chromosome abnormality on male gonad agenesis by interphase FISH

用间期细胞FISH技术快速分析性腺发育不全患者的性染色体数目异常

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

5为异型性染色体（ZW型）；

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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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Study on abnormality of sex chromosome in children

儿童性染色体异常的研究

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The Technical Research of Fluorescence in Situ Hybridization for Detection of Fetal Sex Chromosome on Uncultured Amniotic Fluid Cells in Second Trimester

荧光原位杂交技术用于孕中期未培养羊水细胞胎儿性染色体检测的研究

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

在这些研究结果的基础上，本文对由于性染色体畸变而导致的性别发育异常的机制进行了分析和讨论。

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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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Chromosome Diseases of Human ⅱ. Sex Chromosome Diseases

人类染色体疾病

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This is the first study of the genetic causes of infertility that links a particular sex chromosome meiosis-specific gene to sterility.

这是关于与某个特定性染色体连锁，与减数分裂和不育症有关的基因导致不育的首个研究。

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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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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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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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Based on the model of XY type sex chromosome, the entropy variation regularity of sex linked population equilibrium was studied by using the information theory method.

以XY型性染色体为模型，运用信息论方法研究了性连锁群体平衡的熵变规律。

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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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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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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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Reidentification of the sex chromosome of the salivary gland of Anopheles sinensis

中华按蚊多线染色体中X染色体的重新鉴定

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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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