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Paracentric inversions in human chromosome 7.

作者信息

Schmid M, Haaf T, Zorn M

出版信息

Hum Genet. 1986 Oct;74(2):197-9. doi: 10.1007/BF00282094.

DOI:10.1007/BF00282094
PMID:3770747
Abstract

A paracentric inversion (7)(q11q22) and mosaicism 46,XX/45,X was detected in a female with minor malformations. The same inversion was observed in the mother of the patient. The analysis of high resolution banded chromosomes revealed no visible imbalance in the inverted long arm of the chromosome 7. All published cases of paracentric inversions in the human chromosome 7 are reviewed and the relationship between this inversion and the occurrence of an aneuploidy of the sex chromosomes is discussed.

摘要

相似文献

1
Paracentric inversions in human chromosome 7.
Hum Genet. 1986 Oct;74(2):197-9. doi: 10.1007/BF00282094.
2
Two cases of familial paracentric inversion in man associated with sex chromosome anomaly. 47,XXY,inv(5)(q21q32) and 45,X,inv(7)(q11.3q22.3).
Hum Genet. 1979 Apr 5;47(3):261-8. doi: 10.1007/BF00321018.
3
[A second case of (de novo) paracentric inversion of the short arm of the X chromosome].[X染色体短臂(新发)臂内倒位的第二例]
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4
[Pericentric inversions of chromosomes 1, 9 and 16 in patients with sex chromosome anomalies].[性染色体异常患者中1号、9号和16号染色体的臂间倒位]
Tsitol Genet. 1982;16(1):57-60.
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Long-Term Fragility of Y Chromosomes Is Dominated by Short-Term Resolution of Sexual Antagonism.长期脆弱的 Y 染色体由短期解决的性拮抗所主导。
Genetics. 2017 Dec;207(4):1621-1629. doi: 10.1534/genetics.117.300382. Epub 2017 Oct 11.
6
A case of a paracentric inversion inv(7)(q11q22). Prenatal detection and counselling.
Prenat Diagn. 1981 Jan;1(1):81-4. doi: 10.1002/pd.1970010113.
7
Ullrich-Turner syndrome (45,X/46,X,i[Xq]) in a child with a familial inversion of chromosome 3.一名患有3号染色体家族性倒位的儿童罹患乌尔里希-特纳综合征(45,X/46,X,i[Xq])
Am J Med Genet. 1982 May;12(1):57-62. doi: 10.1002/ajmg.1320120108.
8
Stable dicentric duplication-deficiency chromosome 14 resulting from crossing-over within a maternal paracentric inversion.由母源性臂间倒位内的交叉互换导致的稳定双着丝粒重复-缺失14号染色体
Am J Med Genet. 2002 Dec 15;113(4):333-8. doi: 10.1002/ajmg.b.10720.
9
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10
Recombinant chromosome 7 in a mosaic 45,X/47,XXX patient.一个镶嵌型 45,X/47,XXX 患者的重组 7 号染色体。
Am J Med Genet A. 2012 Jan;158A(1):206-14. doi: 10.1002/ajmg.a.34364. Epub 2011 Nov 21.

引用本文的文献

1
Paracentric inversions: a review.臂间倒位:综述
Hum Genet. 1995 Nov;96(5):503-15. doi: 10.1007/BF00197403.
2
Paracentric inversion in a female with multiple miscarriages (7inv)(q2.13;q3.13).一名有多次流产史女性的臂内倒位(7号染色体,倒位发生在q2.13和q3.13之间)
Hum Genet. 1987 Apr;75(4):391. doi: 10.1007/BF00284116.
3
Genetic markers on chromosome 7.7号染色体上的遗传标记。

本文引用的文献

1
A case of a paracentric inversion inv(7)(q11q22). Prenatal detection and counselling.
Prenat Diagn. 1981 Jan;1(1):81-4. doi: 10.1002/pd.1970010113.
2
Tiny interstitial duplication of proximal 7q in association with a maternal paracentric inversion.近端7q微小间质重复伴母亲臂间倒位。
Hum Genet. 1982;62(2):113-6. doi: 10.1007/BF00282296.
3
A paracentric chromosomal inversion associated with repeated early pregnancy wastage.一种与反复早期妊娠丢失相关的臂内染色体倒位。
Fertil Steril. 1983 Jul;40(1):124-6. doi: 10.1016/s0015-0282(16)47190-6.
J Med Genet. 1988 May;25(5):294-306. doi: 10.1136/jmg.25.5.294.
4
Paracentric inversions: two new familial cases, inv (7)(q22q11) and inv (11)(q23q13).臂内倒位:两例新的家族性病例,inv(7)(q22q11)和inv(11)(q23q13)
J Med Genet. 1983 Jun;20(3):231. doi: 10.1136/jmg.20.3.231.
5
DNA polymerase alpha inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes.阿非科林对DNA聚合酶α的抑制作用会在人类染色体的常见脆性位点诱导缺口和断裂。
Hum Genet. 1984;67(2):136-42. doi: 10.1007/BF00272988.
6
Paracentric inversions in man.人类的臂间倒位
J Med Genet. 1984 Dec;21(6):407-12. doi: 10.1136/jmg.21.6.407.
7
Pericentric inversions. Problems and significance for clinical genetics.臂间倒位。临床遗传学中的问题及意义。
Hum Genet. 1984;68(1):1-47. doi: 10.1007/BF00293869.
8
Identification of human chromosomes by DNA-binding fluorescent agents.利用DNA结合荧光剂鉴定人类染色体
Chromosoma. 1970;30(2):215-27. doi: 10.1007/BF00282002.
9
Pericentric inversions of human chromosomes 9 and 10.人类9号和10号染色体的臂间倒位
Am J Hum Genet. 1974 Nov;26(6):746-66.
10
A simple method for R banding of human chromosomes, showing a pH-dependent connection between R and G bands.一种用于人类染色体R显带的简单方法,显示了R带与G带之间的pH依赖性联系。
Humangenetik. 1974 Jan 22;21(1):55-8. doi: 10.1007/BF00278565.