人类男性减数分裂的细胞遗传学方面 - Suppr

Suppr

超能文献

Cytogenetic aspects of human male meiosis.

作者信息

Hultén M, Lindsten J

出版信息

Adv Hum Genet. 1973;4:327-87. doi: 10.1007/978-1-4615-8261-8_5.

DOI:10.1007/978-1-4615-8261-8_5

PMID:4131530

Abstract

摘要

相似文献

Cytogenetic aspects of human male meiosis.人类男性减数分裂的细胞遗传学方面

Adv Hum Genet. 1973;4:327-87. doi: 10.1007/978-1-4615-8261-8_5.

Chromosomes and human infertility. I. Mitotic and meiotic chromosome studies in 202 consecutive male patients.染色体与人类不育症。I. 对202例男性患者的有丝分裂和减数分裂染色体研究

Clin Genet. 1974;5(2):116-26. doi: 10.1111/j.1399-0004.1974.tb01673.x.

Induction of distinctive chromosomal bands in selected human subjects with D, G, and Y chromosome anomalies.在选定的患有D、G和Y染色体异常的人类受试者中诱导出独特的染色体带。

Hum Hered. 1973 Apr;23(4):313-30. doi: 10.1159/000152592.

Meiosis and spermatogenesis in two postpubertal males with Down's syndrome: 47, XY, G+.

Clin Genet. 1971;2(1):50-7. doi: 10.1111/j.1399-0004.1971.tb00255.x.

A familial Y-autosome translocation in man.人类中的一种家族性Y染色体-常染色体易位。

Clin Genet. 1971;2(1):1-6. doi: 10.1111/j.1399-0004.1971.tb00248.x.

Translocation heterozygosity and associated subfertility in man.人类中的易位杂合性及相关的生育力低下

Cytogenetics. 1972;11(6):516-33. doi: 10.1159/000130218.

Meiosis and spermatogenesis in G-trisomic males.G三体男性的减数分裂与精子发生

Humangenetik. 1971;13(1):15-24. doi: 10.1007/BF00446409.

Spontaneous univalence at male meiosis in the mouse.

Cytogenet Cell Genet. 1973;12(5):327-35. doi: 10.1159/000130471.

Human chromosome abnormalities as related to physical and mental dysfunction.与身心功能障碍相关的人类染色体异常。

J Hered. 1969 Sep-Oct;60(5):239-48. doi: 10.1093/oxfordjournals.jhered.a107981.

A peculiar t(21 ; 14) translocation, associated with a pericentric inversion of the Y chromosome in a mongol boy.一名蒙古男孩中出现一种特殊的t(21;14)易位，并伴有Y染色体的臂间倒位。

Ann Genet. 1974 Sep;17(3):217-20.

引用本文的文献

On the origin of crossover interference: A chromosome oscillatory movement (COM) model.论交叉干涉的起源：一种染色体振荡运动（COM）模型。

Mol Cytogenet. 2011 Apr 8;4:10. doi: 10.1186/1755-8166-4-10.

On the origin of trisomy 21 Down syndrome.关于21三体唐氏综合征的起源

Mol Cytogenet. 2008 Sep 18;1:21. doi: 10.1186/1755-8166-1-21.

Human male recombination maps for individual chromosomes.人类各条染色体的男性重组图谱。

Am J Hum Genet. 2004 Mar;74(3):521-31. doi: 10.1086/382138. Epub 2004 Feb 18.

Meiotic studies of a human male carrier of the common translocation, t(11;22), suggests postzygotic selection rather than preferential 3:1 MI segregation as the cause of liveborn offspring with an unbalanced translocation.对一名常见易位t(11;22)的男性携带者进行的减数分裂研究表明，合子后选择而非3:1的第一次减数分裂优先分离是导致活产后代出现不平衡易位的原因。

Am J Hum Genet. 2000 Sep;67(3):601-9. doi: 10.1086/303052. Epub 2000 Aug 8.

XY chromosome behaviour in the germ-line of the human male: a FISH analysis of spatial orientation, chromatin condensation and pairing.人类男性生殖细胞系中XY染色体的行为：空间取向、染色质凝聚和配对的荧光原位杂交分析

Chromosome Res. 1994 Nov;2(6):445-52. doi: 10.1007/BF01552867.

Chromosome behaviour during early meiotic prophase of mouse primary spermatocytes.小鼠初级精母细胞减数分裂前期早期的染色体行为

Chromosoma. 1981;83(3):395-407. doi: 10.1007/BF00327361.

Ultrastructural changes of the intercellular relationship in impaired human spermatogenesis.人类精子发生受损时细胞间关系的超微结构变化

Hum Genet. 1980;54(3):391-404. doi: 10.1007/BF00291587.

Chiasma distribution, genetic lengths, and recombination fractions: a comparison between chromosomes 15 and 16.交叉分布、遗传长度和重组率：15号与16号染色体的比较

J Med Genet. 1983 Aug;20(4):290-9. doi: 10.1136/jmg.20.4.290.

Synchronous replication of terminal regions of short arms in human X and Y chromosomes.人类X和Y染色体短臂末端区域的同步复制。

Mol Gen Genet. 1984;198(2):55-6. doi: 10.1007/BF00328700.

Studies on chiasma frequency and distribution in two fertile men carrying reciprocal translocations; one with a t(9;10) karyotype and one with a t(Y;10) karyotype.对两名携带相互易位的可育男性的交叉频率和分布的研究；一名为t(9;10)核型，另一名为t(Y;10)核型。

Hum Genet. 1984;68(3):235-47. doi: 10.1007/BF00418394.

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