关于个体近端着丝粒染色体的联合频率与核仁缢痕之间的关系。 - Suppr

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On the relationship between the frequency of association and the nucleolar constriction of individual acrocentric chromosomes.

作者信息

Schmid M, Krone W, Vogel W

出版信息

Humangenetik. 1974;23(4):267-77. doi: 10.1007/BF00272510.

DOI:10.1007/BF00272510

PMID:4138482

Abstract

摘要

相似文献

On the relationship between the frequency of association and the nucleolar constriction of individual acrocentric chromosomes.关于个体近端着丝粒染色体的联合频率与核仁缢痕之间的关系。

Humangenetik. 1974;23(4):267-77. doi: 10.1007/BF00272510.

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.

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.

[Acrocentric chromosome associations in human lymphocytes].[人类淋巴细胞中的近端着丝粒染色体关联]

Tsitologiia. 1972 Sep;14(9):1098-205.

Inheritance of acrocentric association patterns.近端着丝粒联合模式的遗传

Humangenetik. 1975 Oct 7;29(4):309-18. doi: 10.1007/BF00394193.

Acrocentric associations in mongol populations.蒙古人群中的近端着丝粒染色体联合

Humangenetik. 1974 Apr 24;22(1):17-22. doi: 10.1007/BF00338131.

General and specific patterns of acrocentric association in parents of mongol children.蒙古症儿童父母近端着丝粒染色体联合的一般模式和特殊模式。

Humangenetik. 1974;23(4):279-87. doi: 10.1007/BF00272511.

Preferential association of nucleolar organizing human chromosomes as revealed by silver staining technique at mitosis.有丝分裂时银染技术揭示的核仁组织区人类染色体的优先关联

Mol Gen Genet. 1983;190(2):352-4. doi: 10.1007/BF00330664.

[Acrocentric associations in parents of mongol children].[蒙古症儿童父母中的近端着丝粒染色体联合]

Humangenetik. 1974;25(1):29-48.

[Translocations in which nucleolar organizers participate (proceedings)].

An Acad Bras Cienc. 1978 Mar;50(1):118-9.

引用本文的文献

Structural variations of subterminal satellite blocks and their source mechanisms as inferred from the meiotic configurations of chimpanzee chromosome termini.从黑猩猩染色体末端的减数分裂构型推断出末端卫星块的结构变异及其来源机制。

Chromosome Res. 2019 Dec;27(4):321-332. doi: 10.1007/s10577-019-09615-z. Epub 2019 Aug 15.

Variation in pattern and frequency of acrocentric association in normal and trisomy-21 individuals.正常个体和21三体个体近端着丝粒联合的模式和频率变化。

Hum Genet. 1981;59(1):14-22. doi: 10.1007/BF00278848.

Genomic differentiation of 18S ribosomal DNA and beta-satellite DNA in the hominoid and its evolutionary aspects.灵长类动物中18S核糖体DNA和β卫星DNA的基因组分化及其进化方面

Chromosome Res. 1999;7(7):531-40. doi: 10.1023/a:1009237412155.

Nonrandom association of acrocentric chromosomes in human epithelial cells.人类上皮细胞中近端着丝粒染色体的非随机关联。

Experientia. 1981 May 15;37(5):476-8. doi: 10.1007/BF01986144.

Genetic determination of NOR activity in human lymphocytes from twins.双胞胎人类淋巴细胞中核仁组织区活性的遗传决定因素

Hum Genet. 1982;60(1):24-9. doi: 10.1007/BF00281258.

Correlations between relatives for acrocentric association frequency.近端着丝粒染色体关联频率的亲属间相关性。

Hum Genet. 1981;59(3):245-9. doi: 10.1007/BF00283673.

Human inherited marker chromosome 22 short-arm enlargement: investigation of rDNA gene multiplicity, Ag-band size, and acrocentric association.人类遗传性标记染色体22短臂增大：核糖体DNA基因多样性、银染带大小及近端着丝粒关联的研究

Hum Genet. 1981;58(2):135-9. doi: 10.1007/BF00278697.

Satellited Y chromosomes: structure, origin, and clinical significance.随体Y染色体：结构、起源及临床意义

Hum Genet. 1984;67(1):72-85. doi: 10.1007/BF00270562.

NOR activity and satellite association patterns in a family carrying a doubly satellited marker.携带双卫星标记的一个家族中的核仁组织区活性和卫星关联模式。

Hum Genet. 1983;63(3):238-40. doi: 10.1007/BF00284656.

Nucleolus organizer regions and nucleoli.核仁组织区与核仁

Hum Genet. 1983;63(2):89-99. doi: 10.1007/BF00291525.

本文引用的文献

Random association of human acrocentric chromosomes.人类近端着丝粒染色体的随机联合。

Am J Hum Genet. 1969 Sep;21(5):513-5.

New cases of the Oxford nuclear marker in the South African Clawed Toad.

Rev Suisse Zool. 1968 Sep;75(3):506-9.

Quantitative studies on the arrangement of human metaphase chromosomes. I. Individual features in the association pattern of the acrocentric chromosomes of normal males and females.人类中期染色体排列的定量研究。I. 正常男性和女性近端着丝粒染色体联合模式的个体特征。

Cytogenetics. 1968;7(6):455-70.

Satellite associations of D group chromosomes in translocation carriers.易位携带者中D组染色体的卫星联合

J Med Genet. 1970 Dec;7(4):371-3. doi: 10.1136/jmg.7.4.371.

[A case with balanced (14p+; 15p minus)-translocation].[一例平衡型（14号染色体短臂增加；15号染色体短臂缺失）易位病例]

Humangenetik. 1970;8(4):312-20. doi: 10.1007/BF00280330.

Exclusion of marker genes from the short arm of the human chromosome D1 by deletion mapping.

Hereditas. 1969;62(1):116-30.

Number of each type of acrocentric association and probability of its occurrence in human male and female metaphase cells.人类男性和女性中期细胞中每种近端着丝粒联合的数量及其出现的概率。

Cytogenetics. 1969;8(6):439-46. doi: 10.1159/000130055.

The length of secondary chromosomal constrictions in normal individuals and in a nucleolar mutant of Xenopus laevis.正常个体及非洲爪蟾核仁突变体中次级染色体缢痕的长度。

Cytogenetics. 1969;8(6):427-38. doi: 10.1159/000130054.

Variation in the activity of nucleolar organizers and their ribosomal gene content.核仁组织者活性及其核糖体基因含量的变化。

Chromosoma. 1969;28(4):430-44. doi: 10.1007/BF00284259.

Human chromosomology: random association of acrocentrics.人类染色体学：近端着丝粒染色体的随机配对

Genetica. 1970;41(4):626-34. doi: 10.1007/BF00958939.

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