通过银染和原位杂交研究家族性相互易位t(9;13)(p11;p12) - Suppr

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Familial reciprocal translocation t(9;13)(p11;p12) investigated by silver staining and in situ hybridisation.

作者信息

Varley J M, Gosden J, Hultén M

出版信息

Hum Genet. 1981;59(4):422-8. doi: 10.1007/BF00295484.

DOI:10.1007/BF00295484

PMID:6174409

Abstract

摘要

相似文献

Familial reciprocal translocation t(9;13)(p11;p12) investigated by silver staining and in situ hybridisation.通过银染和原位杂交研究家族性相互易位t(9;13)(p11;p12)

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Two reciprocal translocations t(9p+;13q-) and t(13q-;21q+): a study of the families.两个相互易位t(9p+;13q-)和t(13q-;21q+)：家族研究

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Is it always the same NOR that is more active in a pair of acrocentrics with distinct AG-stainings?在一对具有不同AG染色的近端着丝粒染色体中，总是同一个核仁组织区（NOR）更活跃吗？

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[Nucleolus organizer region--centromere translocation].

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[Frequency of Ag-stained NOR and satellite associations in four 14/21 translocation carriers and in their normal relatives (author's transl)].四名14/21易位携带者及其正常亲属中银染核仁组织区（NOR）和随体联合的频率（作者译）

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A familial insertion involving an active nucleolar organiser within chromosome 12.一个涉及12号染色体内活性核仁组织区的家族性插入。

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Translocation t(11;14) and trisomy 11q13----qter in multiple myeloma.

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引用本文的文献

Cytogenetic and molecular analyses of de novo translocation dic(9;13)(p11.2;p12) in an infertile male.一名不育男性新发9号与13号染色体易位dic(9;13)(p11.2;p12)的细胞遗传学和分子分析

Mol Cytogenet. 2014 Feb 21;7(1):14. doi: 10.1186/1755-8166-7-14.

A familial insertion involving an active nucleolar organiser within chromosome 12.一个涉及12号染色体内活性核仁组织区的家族性插入。

J Med Genet. 1984 Oct;21(5):379-84. doi: 10.1136/jmg.21.5.379.

Outcome after prenatal detection of a sporadic, unstable translocation t(5;21).

J Med Genet. 1986 Jun;23(3):274-8. doi: 10.1136/jmg.23.3.274.

Inheritance of ribosomal gene activity and level of DNA methylation of individual gene clusters in a three generation family.

Hum Genet. 1991 Dec;88(2):146-52. doi: 10.1007/BF00206062.

A molecular deletion of distal chromosome 4p in two families with a satellited chromosome 4 lacking the Wolf-Hirschhorn syndrome phenotype.两个家族中4号染色体远端分子缺失伴卫星4号染色体，无Wolf-Hirschhorn综合征表型。

Am J Hum Genet. 1992 Nov;51(5):971-8.

本文引用的文献

THE ASSOCIATION OF SATELLITED CHROMOSOMES WITH SPECIFIC CHROMOSOMAL REGIONS IN CULTURED HUMAN SOMATIC CELLS.培养的人体体细胞中卫星染色体与特定染色体区域的关联

Ann Hum Genet. 1963 Nov;27:143-56. doi: 10.1111/j.1469-1809.1963.tb00207.x.

Observations on the satellited human chromosomes.关于人类随体染色体的观察

Lancet. 1961 Mar 25;1(7178):638-40. doi: 10.1016/s0140-6736(61)91655-5.

NOR activity in two families with balanced D;D translocations and numerous consecutive miscarriages.

Hereditas. 1980;92(2):217-21. doi: 10.1111/j.1601-5223.1980.tb01699.x.

The identification of human chromosomes by quinacrine fluorescence after hybridisation in situ.原位杂交后用喹吖因荧光法鉴定人类染色体。

Hum Genet. 1980;53(3):371-3. doi: 10.1007/BF00287058.

Nucleolus organizer regions in translocations involving acrocentric chromosomes.涉及近端着丝粒染色体易位中的核仁组织区。

Cytogenet Cell Genet. 1980;26(1):14-21. doi: 10.1159/000131416.

Satellite DNA and cytological staining patterns in heterochromatic inversions of human chromosome 9.人类9号染色体异染色质倒位中的卫星DNA和细胞学染色模式

Hum Genet. 1981;58(3):276-8. doi: 10.1007/BF00294922.

Satellite DNA sequences in the human acrocentric chromosomes: information from translocations and heteromorphisms.人类近端着丝粒染色体中的卫星DNA序列：来自易位和异态性的信息。

Am J Hum Genet. 1981 Mar;33(2):243-51.

[4 cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity].4例9号染色体短臂三体。一种新的病态实体的个体化研究

Ann Genet. 1970 Dec;13(4):217-32.

Pericentric inversions of chromosome 9 in two families.两个家族中9号染色体的臂间倒位

Cytogenetics. 1972;11(2):132-44. doi: 10.1159/000130182.

Trisomy 9 mosaicism in a newborn infant with multiple malformations.一名患有多种畸形的新生儿的9号染色体三体嵌合体。

J Pediatr. 1974 Jul;85(1):95-7. doi: 10.1016/s0022-3476(74)80297-0.

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