XO特纳综合征中单一X染色体的来源：一则评论 - Suppr

Suppr

超能文献

Source of single X in XO Turner syndrome: a comment.

作者信息

Tippett P, Sanger R

出版信息

Hum Genet. 1985;70(1):92. doi: 10.1007/BF00389469.

DOI:10.1007/BF00389469

PMID:3997157

Abstract

摘要

相似文献

Source of single X in XO Turner syndrome: a comment.

Hum Genet. 1985;70(1):92. doi: 10.1007/BF00389469.

[A case of 45,XO/46,X,r(X). A brief clinical communication].

Sb Lek. 1987 Feb-Mar;89(2-3):73-5.

Genotype, phenotype, and karyotype correlation in the XO mouse model of Turner Syndrome.

J Hered. 2008 Sep-Oct;99(5):512-7. doi: 10.1093/jhered/esn027. Epub 2008 May 21.

Are all phenotypically-normal Turner syndrome fetuses mosaics?

Prenat Diagn. 1996 Sep;16(9):791-5. doi: 10.1002/(SICI)1097-0223(199609)16:9<791::AID-PD944>3.0.CO;2-3.

The 39,XO mouse as a model for the neurobiology of Turner syndrome and sex-biased neuropsychiatric disorders.

Behav Brain Res. 2007 May 16;179(2):173-82. doi: 10.1016/j.bbr.2007.02.013. Epub 2007 Feb 20.

[Turner' syndrome (monosomy) and pregnancy].

Zentralbl Gynakol. 2000;122(2):103-5.

Prenatal selection in XO mice.

Nature. 1991 Oct 24;353(6346):709. doi: 10.1038/353709a0.

Rearrangements of the X chromosome and Turner syndrome.

Hum Genet. 1992 Sep-Oct;90(1-2):185-6. doi: 10.1007/BF00210774.

Identification of a cluster of X-linked imprinted genes in mice.

Nat Genet. 2005 Jun;37(6):620-4. doi: 10.1038/ng1567. Epub 2005 May 22.

[XO type of Turner's syndrome associated with coarctation of aorta---case report (author's transl)].

Zhonghua Xin Xue Guan Bing Za Zhi. 1980 Sep;8(3):208-9.

引用本文的文献

On the origin of chromosome anomaly.

Am J Hum Genet. 1988 Apr;42(4):529-33.

Cytogenetic and molecular analysis of sex-chromosome monosomy.

Am J Hum Genet. 1988 Apr;42(4):534-41.

De novo DNA microdeletion in a girl with Turner syndrome and Duchenne muscular dystrophy.

Hum Genet. 1986 Oct;74(2):193-6. doi: 10.1007/BF00282093.

Analysis of non-disjunction in sex chromosome tetrasomy and pentasomy.

Hum Genet. 1990 Oct;85(6):648-50. doi: 10.1007/BF00193591.

本文引用的文献

Parental origin of the sex chromosomes in the XO and XXY karyotypes in man.

Ann Hum Genet. 1963 Jun;26:297-304. doi: 10.1111/j.1469-1809.1963.tb01325.x.

Excess paternal meiotic errors in Turner syndrome: natural result of ascertainment bias.

Hum Genet. 1984;67(3):347-8. doi: 10.1007/BF00291367.

Xg groups and sex abnormalities in people of northern European ancestry.

J Med Genet. 1971 Dec;8(4):417-26. doi: 10.1136/jmg.8.4.417.

Xg groups and sex chromosome abnormalities in people of northern European ancestry: an addendum.

J Med Genet. 1977 Jun;14(3):210-1. doi: 10.1136/jmg.14.3.210.

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