一条稳定的人类双着丝粒染色体，t dic(12;14)(p13;p13)，其着丝粒之间包含一个中间卫星区域。 - Suppr

Suppr

超能文献

A stable human dicentric chromosome, t dic (12;14)(p13;p13) including an intercalary satellite region between centromeres.

作者信息

Warburton D, Henderson A S, Shapiro L R, Hsu L Y

出版信息

Am J Hum Genet. 1973 Jul;25(4):439-45.

PMID:4716663

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1762447/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21f3/1762447/6c5b511aee89/ajhg00449-0097-a.jpg

相似文献

A stable human dicentric chromosome, t dic (12;14)(p13;p13) including an intercalary satellite region between centromeres.一条稳定的人类双着丝粒染色体，t dic(12;14)(p13;p13)，其着丝粒之间包含一个中间卫星区域。

Am J Hum Genet. 1973 Jul;25(4):439-45.

Dicentric chromosome 13 and centromere inactivation.双着丝粒13号染色体与着丝粒失活

Hum Genet. 1983;63(4):332-7. doi: 10.1007/BF00274757.

Human chromosome identification and the pattern of DNA replication in fibroblasts from an XXY male. A quantitative autoradiographic study of early and late synthesis.XXY男性成纤维细胞中的人类染色体鉴定及DNA复制模式。早期和晚期合成的定量放射自显影研究。

Cytogenetics. 1969;8(4):272-95.

Cytogenetics. 1969;8(5):272-95.

Pericentric inversion in a group D chromosome (13-15) associated with amenorrhea and gonadal dysgenesis.与闭经和性腺发育不全相关的D组染色体（13 - 15）臂间倒位。

Ann Hum Genet. 1967 May;30(4):313-23. doi: 10.1111/j.1469-1809.1967.tb00032.x.

Chromosome studies on women who have had two or more unsuccessful pregnancies.

J Obstet Gynaecol Br Commonw. 1968 Jan;75(1):66-70. doi: 10.1111/j.1471-0528.1968.tb00122.x.

[Clinical and cytogenetic findings in a rare autosomal aberrations].[罕见常染色体畸变的临床和细胞遗传学发现]

Monatsschr Kinderheilkd (1902). 1970 Jun;118(6):308-13.

Smaller G (Gp-) and t (Gp-; Dp+) chromosomes. A familial study with one member having acute leukemia.

Am J Dis Child. 1968 Jun;115(6):732-8.

[Gonadal agenesia 46, XX. Presence of a familial double satellite on a chromosome of the D group].[性腺发育不全，46，XX。D组染色体上存在家族性双随体]

Bull Fed Soc Gynecol Obstet Lang Fr. 1970 Jan-Mar;22(1):106-10.

Trisomy for the short arm of chromosome No. 10.10号染色体短臂三体性

Clin Genet. 1974;6(5):408-15. doi: 10.1111/j.1399-0004.1974.tb02264.x.

引用本文的文献

Mixed gonadal dysgenesis in a patient with de novo tas(Y;19)(p11.3;q13.4) and 45,X mosaicism.患者存在新发 tas(Y;19)(p11.3;q13.4)和 45,X 嵌合体，患有混合性性腺发育不全。

Eur J Pediatr. 2013 Sep;172(9):1215-9. doi: 10.1007/s00431-013-2028-1. Epub 2013 May 8.

Molecular cytogenetic characterization of a non-robertsonian dicentric chromosome 14;19 identified in a girl with short stature and amenorrhea.在一名身材矮小和闭经的女孩中鉴定出的一条非罗伯逊双着丝粒14;19号染色体的分子细胞遗传学特征。

Case Rep Genet. 2012;2012:212065. doi: 10.1155/2012/212065. Epub 2012 Nov 5.

Dicentric chromosomes: unique models to study centromere function and inactivation.着丝粒染色体：研究着丝粒功能和失活的独特模型。

Chromosome Res. 2012 Jul;20(5):595-605. doi: 10.1007/s10577-012-9302-3.

2006 William Allan Award Address. Having it all.2006年威廉·艾伦奖获奖致辞。拥有一切。

Am J Hum Genet. 2007 Oct;81(4):648-56. doi: 10.1086/521405.

A stable dicentric chromosome: both centromeres develop kinetochores and attach to the spindle in monocentric and dicentric configuration.一条稳定的双着丝粒染色体：两个着丝粒都形成动粒，并以单着丝粒和双着丝粒构型附着于纺锤体。

Chromosoma. 1994 Mar;103(1):56-62. doi: 10.1007/BF00364726.

Analysis of centromeric activity in Robertsonian translocations: implications for a functional acrocentric hierarchy.罗伯逊易位中着丝粒活性的分析：对功能性近端着丝粒等级制度的影响。

Chromosoma. 1994 Dec;103(7):459-67. doi: 10.1007/BF00337384.

Apparently isodicentric but functionally monocentric X chromosome in man.人类中明显等臂双着丝粒但功能上为单着丝粒的X染色体。

Am J Hum Genet. 1974 Jan;26(1):83-92.

Visualization of centromere proteins CENP-B and CENP-C on a stable dicentric chromosome in cytological spreads.在细胞学涂片的稳定双着丝粒染色体上对着丝粒蛋白CENP - B和CENP - C进行可视化观察。

Chromosoma. 1989 Jun;98(1):1-12. doi: 10.1007/BF00293329.

Dicentric X isochromosomes in man.人类中的双着丝粒X等臂染色体。

J Med Genet. 1976 Dec;13(6):496-500. doi: 10.1136/jmg.13.6.496.

Fusion of two apparently intact human X chromosomes.两条明显完整的人类X染色体融合。

Hum Genet. 1976 Jun 29;32(3):295-300. doi: 10.1007/BF00295819.

本文引用的文献

A Transmissible Dicentric Chromosome.一种可传播的双着丝粒染色体。

Genetics. 1952 Mar;37(2):125-35. doi: 10.1093/genetics/37.2.125.

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.

Quinacrine fluorescence of variant and abnormal human Y chromosomes.变异和异常人类Y染色体的喹吖因荧光

Chromosoma. 1971;35(3):342-52. doi: 10.1007/BF00326283.

Location of ribosomal DNA in the human chromosome complement.核糖体DNA在人类染色体组中的定位。

Proc Natl Acad Sci U S A. 1972 Nov;69(11):3394-8. doi: 10.1073/pnas.69.11.3394.

Translocations causing non-fluorescent Y chromosomes in human XO/XY mosaics.导致人类XO/XY嵌合体中出现非荧光Y染色体的易位。

Hereditas. 1971;68(2):317-24. doi: 10.1111/j.1601-5223.1971.tb02407.x.

An abnormal large human chromosome identified as an end-to-end fusion of two X's by combined results of the new banding techniques and microdensitometry.通过新的显带技术和显微密度测定法的联合结果，鉴定出一条异常大的人类染色体，它是由两条X染色体端对端融合而成。

Clin Genet. 1972;3(5):388-95. doi: 10.1111/j.1399-0004.1972.tb01472.x.

Dicentric and monocentric Robertsonian translocations in man.人类中的双着丝粒和单着丝粒罗伯逊易位

Humangenetik. 1972;16(3):217-26. doi: 10.1007/BF00273467.

Unusual findings by fluorescence microscopy of a t(13q14q).

Humangenetik. 1972;15(1):96-8. doi: 10.1007/BF00273440.

Fluorescence pattern of a dicentric Y.双着丝粒Y染色体的荧光模式。

Humangenetik. 1971;12(2):170-2. doi: 10.1007/BF00291474.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验