人类核仁组织区（NOR）的生化与细胞遗传学研究。I. 21三体与平衡易位t（DqGq）的比较。 - Suppr

Suppr

超能文献

Biochemical and cytogenetic studies on the nucleolus organizing regions (NOR) of man. I. Comparison of trisomy 21 with balanced translocations t(DqGq).

作者信息

Bross K, Dittes H, Krone W, Schmid M, Vogel W

出版信息

Humangenetik. 1973 Dec 10;20(3):223-9. doi: 10.1007/BF00385734.

DOI:10.1007/BF00385734

PMID:4772076

Abstract

摘要

相似文献

Biochemical and cytogenetic studies on the nucleolus organizing regions (NOR) of man. I. Comparison of trisomy 21 with balanced translocations t(DqGq).人类核仁组织区（NOR）的生化与细胞遗传学研究。I. 21三体与平衡易位t（DqGq）的比较。

Humangenetik. 1973 Dec 10;20(3):223-9. doi: 10.1007/BF00385734.

Ribosomal cistrons and acrocentric chromosomes in man.人类的核糖体顺反子和近端着丝粒染色体。

Humangenetik. 1973 Mar 23;18(1):71-5. doi: 10.1007/BF00279033.

Biochemical and cytogenetic studies on the nucleolus organizing regions (NOR) of man. II. A family with the 15/21 translocation.人类核仁组织区（NOR）的生化与细胞遗传学研究。II. 一个具有15/21易位的家系。

Humangenetik. 1975;26(1):47-59. doi: 10.1007/BF00280284.

Familial translocation with partial trisomy of 13 and 22: evidence that specific regions of chromosomes 13 and 22 are responsible for the phenotype of each trisomy.伴有13号和22号染色体部分三体的家族性易位：证据表明13号和22号染色体的特定区域分别导致了各三体的表型。

J Med Genet. 1977 Apr;14(2):114-9. doi: 10.1136/jmg.14.2.114.

Analysis of a transmitted t (DqGq) chromosome in the D1 trisomy family.

Jinrui Idengaku Zasshi. 1974 Jun;19(1):83-4.

Transmission of a t(13q22q) chromosome observed in three generations with segregation of the translocation D1-trisomy syndrome.在三代人中观察到13号染色体长臂2区与22号染色体之间的易位，并伴有易位型D1-三体综合征的分离。

Humangenetik. 1975 Sep 20;30(3):207-15. doi: 10.1007/BF00279186.

[Incorporation of H3-uridine in vitro into normal lymphocytes and those in cases of aberration of acrocentric chromosomes].[体外将H3-尿苷掺入正常淋巴细胞以及近端着丝粒染色体畸变病例的淋巴细胞中]

Probl Med Wieku Rozwoj. 1979;8:101-16.

Segregation of two independent chromosomal translocations in one family.

Hum Genet. 1984;68(1):93-5. doi: 10.1007/BF00293881.

rDNA and acrocentric chromosomes in man.人类的核糖体DNA与近端着丝粒染色体。

Cell Differ. 1974 Mar;2(6):319-24. doi: 10.1016/0045-6039(74)90010-4.

Cat eye syndrome. Partial trisomy 22 due to translocation in the mother.猫眼综合征。因母亲发生染色体易位导致的22号染色体部分三体。

Am J Dis Child. 1977 Aug;131(8):893-97. doi: 10.1001/archpedi.1977.02120210071015.

引用本文的文献

Assessing Human Ribosomal DNA Variation and Its Association With Phenotypic Outcomes.评估人类核糖体DNA变异及其与表型结果的关联。

Bioessays. 2025 Apr;47(4):e202400232. doi: 10.1002/bies.202400232. Epub 2025 Jan 20.

Dosage effects of human ribosomal genes (rDNA) in health and disease.人核糖体基因（rDNA）在健康和疾病中的剂量效应。

Chromosome Res. 2019 Mar;27(1-2):5-17. doi: 10.1007/s10577-018-9587-y. Epub 2018 Oct 20.

Quantitative studies on the arrangement of human metaphase chromosomes. IV. The association frequency of human acrocentric marker chromosomes.人类中期染色体排列的定量研究。IV. 人类近端着丝粒标记染色体的联合频率。

Humangenetik. 1974;23(4):259-65. doi: 10.1007/BF00272509.

Monosomy 21 in a human spontaneous abortus. Morphogenetic disturbances and phenotype at the cellular level.

Hum Genet. 1977 Sep 22;38(2):137-45. doi: 10.1007/BF00527395.

Interferon effect on ribosomal ribonucleic acid related to chromosome 21 ploidy.干扰素对与21号染色体倍性相关的核糖体核糖核酸的影响。

Biochem J. 1979 Apr 1;179(1):221-5. doi: 10.1042/bj1790221.

Human karyotype polymorphism. III. Routine ank fluorescence microscopic investigation of chromosomes in normal adults and mentally retarded children.人类染色体核型多态性。III. 正常成年人和智力发育迟缓儿童染色体的常规银染荧光显微镜检查

Humangenetik. 1975;26(1):1-23. doi: 10.1007/BF00280281.

Humangenetik. 1975;26(1):47-59. doi: 10.1007/BF00280284.

本文引用的文献

Para-nucleolar position of the human Y chromosome in interphase nuclei.人类Y染色体在间期细胞核中的副核仁位置。

Nature. 1971 Aug 20;232(5312):556-7. doi: 10.1038/232556a0.

Ribosomal cistrons and acrocentric chromosomes in man.人类的核糖体顺反子和近端着丝粒染色体。

Humangenetik. 1973 Mar 23;18(1):71-5. doi: 10.1007/BF00279033.

Kinetic complexity of RNA molecules.RNA分子的动力学复杂性。

J Mol Biol. 1972 Jan 14;63(1):21-39. doi: 10.1016/0022-2836(72)90519-0.

Protein and RNA synthesis in trisomic Down's syndrome leucocytes.三体性唐氏综合征白细胞中的蛋白质和RNA合成

Nature. 1967 Sep 16;215(5107):1290-1. doi: 10.1038/2151290a0.

Polymorphism of human C-band heterochromatin. I. Frequency of variants.人类C带异染色质的多态性。I. 变异体的频率。

Am J Hum Genet. 1973 Mar;25(2):181-92.

Localization of heterochromatin in human chromosomes.人类染色体中异染色质的定位

Cytogenetics. 1971;10(2):81-6. doi: 10.1159/000130130.

Identification of G group anomalies in Down's syndrome by quinacrine dihydrochloride fluorescence staining.用盐酸阿的平荧光染色法鉴定唐氏综合征中的G组异常。

Humangenetik. 1971;12(1):67-73. doi: 10.1007/BF00291036.

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