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自然流产的细胞遗传学研究:卡尔加里的经验

Cytogenetic studies in spontaneous abortion: the Calgary experience.

作者信息

Lin C C, De Braekeleer M, Jamro H

出版信息

Can J Genet Cytol. 1985 Oct;27(5):565-70. doi: 10.1139/g85-083.

DOI:10.1139/g85-083
PMID:4063875
Abstract

In a series of 493 apparently consecutive products of spontaneous abortions obtained for cytogenetic studies, tissue culture was attempted in 428 cases; chromosome analysis using the Q-banding technique was completed in 215 cases (50.2%). Abnormal karyotypes were identified in 80 cases (37.2%). Maternal tissue contamination was apparent and the actual frequency of karyotypic abnormal abortuses could be as high as 50%. Comparison of the frequency of a specific type of chromosome abnormalities with nine other series of studies showed the lowest frequency of autosomal trisomies and the highest frequency of triploidies and structural aberrations in the Calgary series. In addition, a significantly lower gestational age was observed for triploidies 69, XXX as compared to the 69, XXY.

摘要

在为细胞遗传学研究获取的一系列493例明显连续的自然流产产物中,对428例进行了组织培养尝试;采用Q显带技术完成了215例(50.2%)的染色体分析。在80例(37.2%)中鉴定出异常核型。母体组织污染明显,核型异常流产的实际发生率可能高达50%。将一种特定类型的染色体异常频率与其他九项系列研究进行比较,结果显示卡尔加里系列中常染色体三体的频率最低,三倍体和结构畸变的频率最高。此外,与69, XXY三倍体相比,观察到69, XXX三倍体的妊娠年龄明显更低。

相似文献

1
Cytogenetic studies in spontaneous abortion: the Calgary experience.自然流产的细胞遗传学研究:卡尔加里的经验
Can J Genet Cytol. 1985 Oct;27(5):565-70. doi: 10.1139/g85-083.
2
Cytogenetic studies in spontaneous abortuses.自然流产的细胞遗传学研究。
Hum Genet. 1984;66(1):77-84. doi: 10.1007/BF00275191.
3
Q-banding of chromosomes in human spontaneous abortions.人类自然流产中染色体的Q带分析
Can J Genet Cytol. 1978 Sep;20(3):415-25. doi: 10.1139/g78-048.
4
[Clinical experience and possibilities of rapid cytogenetic diagnosis of spontaneous abortions in the routine work load of a gynecology clinic].[妇科门诊日常工作量中自然流产快速细胞遗传学诊断的临床经验及可能性]
Geburtshilfe Frauenheilkd. 1991 Jun;51(6):450-3. doi: 10.1055/s-2007-1026176.
5
The significance of oral contraceptives in causing chromosome anomalies in spontaneous abortions.口服避孕药在导致自然流产染色体异常方面的意义。
Acta Obstet Gynecol Scand. 1975;54(3):261-4. doi: 10.3109/00016347509157773.
6
[Cytogenetic studies of spontaneous abortions in humans].[人类自然流产的细胞遗传学研究]
Zhonghua Fu Chan Ke Za Zhi. 1990 Mar;25(2):89-91, 124.
7
Incidence of numerical chromosome anomalies in human pregnancy estimation from induced and spontaneous abortion data.根据人工流产和自然流产数据估算人类妊娠中染色体数目异常的发生率。
Hum Reprod. 1991 Apr;6(4):555-65. doi: 10.1093/oxfordjournals.humrep.a137379.
8
[Spontaneous abortion and genetic natural selection].[自然流产与基因自然选择]
Orv Hetil. 1993 Jul 4;134(27):1459-64.
9
[Chromosomal disorders in women with spontaneous abortions].
Genetika. 1988 Jul;24(7):1314-6.
10
A cytogenetic study of human spontaneous abortions using banding techniques.一项运用显带技术对人类自然流产进行的细胞遗传学研究。
Hum Genet. 1976 Feb 29;31(2):177-96. doi: 10.1007/BF00296145.

引用本文的文献

1
Prevalence of chromosomal alterations in first-trimester spontaneous pregnancy loss.早孕期自然流产中染色体异常的发生率。
Nat Med. 2023 Dec;29(12):3233-3242. doi: 10.1038/s41591-023-02645-5. Epub 2023 Nov 23.
2
Rescue karyotyping: a case series of array-based comparative genomic hybridization evaluation of archival conceptual tissue.挽救性核型分析:一系列基于阵列的比较基因组杂交对存档概念性组织的评估病例
Reprod Biol Endocrinol. 2014 Mar 3;12:19. doi: 10.1186/1477-7827-12-19.
3
Array-based comparative genomic hybridization is more informative than conventional karyotyping and fluorescence in situ hybridization in the analysis of first-trimester spontaneous abortion.
在孕早期自然流产的分析中,基于芯片的比较基因组杂交比传统的核型分析和荧光原位杂交提供的信息更多。
Mol Cytogenet. 2012 Jul 16;5(1):33. doi: 10.1186/1755-8166-5-33.