性染色体非整倍体的起源。 - Suppr

Suppr

超能文献

The origin of sex chromosome aneuploidy.

作者信息

Jacobs P, Hassold T, Harvey J, May K

机构信息

Wessex Regional Cytogenetic Unit S.G.I., Salisbury, Wilts U.K.

出版信息

Prog Clin Biol Res. 1989;311:135-51.

PMID:2528150

Abstract

摘要

相似文献

The origin of sex chromosome aneuploidy.性染色体非整倍体的起源。

Prog Clin Biol Res. 1989;311:135-51.

Double aneuploidy (48,XXY,+21) of maternal origin in a child born to a 13-year-old mother: evaluation of the maternal folate metabolism.一名13岁母亲所生孩子中源自母亲的双非整倍体（48,XXY,+21）：母亲叶酸代谢评估

Genet Couns. 2009;20(3):225-34.

Summary of clinical findings: profiles of children with 47,XXY, 47,XXX and 47,XYY karyotypes.临床发现总结：47,XXY、47,XXX和47,XYY核型儿童的概况。

Birth Defects Orig Artic Ser. 1979;15(1):261-6.

The parental origin of the missing or additional chromosome in 45,X and 47,XXX females.45,X和47,XXX女性中缺失或额外染色体的亲本来源。

Birth Defects Orig Artic Ser. 1990;26(4):297-304.

[Chromosomal factors in sterility in men].

Akush Ginekol (Sofiia). 1984;23(1):88-93.

Double aneuploidy in three Egyptian patients: Down-Turner and Down-Klinefelter syndromes.三名埃及患者的双非整倍体：唐氏-特纳综合征和唐氏-克兰费尔特综合征。

Genet Couns. 2005;16(4):393-402.

Occurrence of aneuploidy for the X chromosome in over 1,300 unrelated specimens screened for the fragile X chromosome.

Am J Med Genet. 1994 Jul 15;51(4):452-3. doi: 10.1002/ajmg.1320510430.

Down anomaly: new research aspects of an old and well known syndrome.唐氏综合征：一种古老且广为人知的综合征的新研究方面

Prog Clin Biol Res. 1985;177:293-307.

To err (meiotically) is human: the genesis of human aneuploidy.（减数分裂时）犯错乃人之常情：人类非整倍体的起源。

Nat Rev Genet. 2001 Apr;2(4):280-91. doi: 10.1038/35066065.

Genetic risk factors in human trisomy 21.人类21三体综合征中的遗传风险因素。

Prog Clin Biol Res. 1989;311:183-97.

引用本文的文献

At Term, XmO and XpO Mouse Placentas Show Differences in Glucose Metabolism in the Trophectoderm-Derived Outer Zone.足月时，XmO和XpO小鼠胎盘在滋养外胚层衍生的外层区域的葡萄糖代谢存在差异。

Front Cell Dev Biol. 2017 Jun 21;5:63. doi: 10.3389/fcell.2017.00063. eCollection 2017.

Occupational exposure to benzene and chromosomal structural aberrations in the sperm of Chinese men.职业性接触苯与中国男性精子染色体结构异常。

Environ Health Perspect. 2012 Feb;120(2):229-34. doi: 10.1289/ehp.1103921. Epub 2011 Nov 15.

Paternally inherited chromosomal structural aberrations detected in mouse first-cleavage zygote metaphases by multicolour fluorescence in situ hybridization painting.通过多色荧光原位杂交染色体涂染技术在小鼠第一次卵裂期受精卵中期检测到的父系遗传染色体结构畸变。

Chromosome Res. 1996 Dec;4(8):604-13. doi: 10.1007/BF02261723.

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验