通过对未受精的体外受精卵母细胞进行细胞遗传学分析检测到的一名45,X/46,XX/47,XXX女性嵌合体。 - Suppr

Suppr

超能文献

A 45,X/46,XX/47,XXX female mosaic detected by cytogenetic analysis of unfertilized IVF oocytes.

作者信息

De Sutter P, Dhont M, Merchiers E, Coetsier T, Verschraegen-Spae M R, Coppens M

机构信息

Gent University Center for Infertility, Belgium.

出版信息

J Assist Reprod Genet. 1993 Aug;10(6):434-7. doi: 10.1007/BF01228094.

DOI:10.1007/BF01228094

PMID:8019092

Abstract

摘要

相似文献

A 45,X/46,XX/47,XXX female mosaic detected by cytogenetic analysis of unfertilized IVF oocytes.通过对未受精的体外受精卵母细胞进行细胞遗传学分析检测到的一名45,X/46,XX/47,XXX女性嵌合体。

J Assist Reprod Genet. 1993 Aug;10(6):434-7. doi: 10.1007/BF01228094.

[Cytogenetic analysis of unfertilized human oocytes].

Tsitol Genet. 2003 Nov-Dec;37(6):60-5.

Cytogenetic abnormalities of unfertilized oocytes generated from in-vitro fertilization and intracytoplasmic sperm injection: a double-blind study.体外受精和卵胞浆内单精子注射产生的未受精卵母细胞的细胞遗传学异常：一项双盲研究。

Hum Reprod. 1997 Dec;12(12):2784-91. doi: 10.1093/humrep/12.12.2784.

Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysis.一名患有15号染色体三体嵌合体和X染色体三体嵌合体的儿童的普拉德-威利综合征：分子分析

J Med Genet. 1997 Apr;34(4):318-22. doi: 10.1136/jmg.34.4.318.

Karyotype 69,XXX/47,XX,+15 in a 2 1/2 year old child.一名2岁半儿童的核型为69,XXX/47,XX,+15 。

J Med Genet. 1997 Mar;34(3):246-9. doi: 10.1136/jmg.34.3.246.

Cytogenetic analysis of unfertilized human oocytes.未受精人类卵母细胞的细胞遗传学分析

Hum Reprod. 1991 Apr;6(4):568-73. doi: 10.1093/oxfordjournals.humrep.a137381.

Chromosomes of oocytes failing in-vitro fertilization.

Hum Reprod. 1995 Oct;10(10):2570-5. doi: 10.1093/oxfordjournals.humrep.a135747.

A case of juvenile chronic myeloid leukemia with XX/XXX mosaicism.

Turk J Pediatr. 1992 Oct-Dec;34(4):251-4.

[Monosomy X in the mosaic. I(XO-XX, XO-XXX, XO-XX-XXX)].

Bratisl Lek Listy. 1969;51(6):725-33.

Chromosome analysis of human oocytes and embryos: does delayed fertilization increase chromosome imbalance?

Hum Reprod. 1988 Jan;3(1):125-7. doi: 10.1093/oxfordjournals.humrep.a136644.

本文引用的文献

Reduced fertility in women with X chromosome abnormality.

Clin Genet. 1984 Apr;25(4):301-9. doi: 10.1111/j.1399-0004.1984.tb01994.x.

Occurrence of sex chromosome mosaicism and translocation Down's syndrome in the same family.

Clin Genet. 1980 May;17(5):341-8. doi: 10.1111/j.1399-0004.1980.tb00160.x.

Isolation and characterization of a major tandem repeat family from the human X chromosome.人类X染色体上一个主要串联重复序列家族的分离与特性分析。

Nucleic Acids Res. 1983 Apr 11;11(7):2017-33. doi: 10.1093/nar/11.7.2017.

Chromosome aberrations in 500 couples referred for in-vitro fertilization or related fertility treatment.500对因体外受精或相关生育治疗前来就诊的夫妇的染色体畸变情况。

Hum Reprod. 1988 May;3(4):451-7. doi: 10.1093/oxfordjournals.humrep.a136726.

Assessment of aneuploidy in the human female by using cytogenetics of IVF failures.通过体外受精失败的细胞遗传学评估人类女性的非整倍体情况。

Am J Hum Genet. 1988 Feb;42(2):274-83.

[Turner's syndrome and pregnancy].

Rev Fr Gynecol Obstet. 1988 Nov;83(11):717-21.

Familial sex chromosomal mosaicism.

Am J Med Genet. 1990 Sep;37(1):15-7. doi: 10.1002/ajmg.1320370105.

Identification and characterization of normal length nonfluorescent Y chromosomes: cytogenetic analysis, southern hybridization and non-isotopic in situ hybridization.正常长度非荧光Y染色体的鉴定与特征分析：细胞遗传学分析、Southern杂交及非同位素原位杂交

Hum Genet. 1990 Oct;85(6):569-75. doi: 10.1007/BF00193576.

Frequency and distribution of aneuploidy in human female gametes.人类雌性配子中非整倍体的频率与分布

Hum Genet. 1991 Jan;86(3):283-8. doi: 10.1007/BF00202410.

Chromosomal analysis in Japanese couples with repeated spontaneous abortions.对反复自然流产的日本夫妇进行的染色体分析。

Int J Fertil. 1990 Sep-Oct;35(5):266-70.

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