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600名希腊受试者的9号染色体多态性

Polymorphism of chromosome 9 in 600 Greek subjects.

作者信息

Metaxotou C, Kalpini-Mavrou A, Panagou M, Tsenghi C

出版信息

Am J Hum Genet. 1978 Jan;30(1):85-9.

PMID:623106
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1685456/
Abstract

The morphologic variations of C-band heterochromatin of chromosome 9 were studied in 600 Greek subjects referred for cytogenetic investigation. There was great variability in the location and length of the heterochromatic bands. The location and length of the heterochromatic band were equal in 177 individuals and unequal in 423. Twenty-five subjects (4%) carried a pericentric inversion on one of the homologs, and 12 individuals (2%) had an extremely elongated C-band in one homolog 9. Our findings are compared with those reported in the literature, and the ethnic variation is discussed and evaluated.

摘要

对600名接受细胞遗传学检查的希腊受试者的9号染色体C带异染色质的形态变异进行了研究。异染色质带的位置和长度存在很大差异。177名个体的异染色质带位置和长度相等,423名个体的则不相等。25名受试者(4%)在其中一条同源染色体上携带了一个臂间倒位,12名个体(2%)的一条9号同源染色体上有一条极其细长的C带。我们将研究结果与文献报道的结果进行了比较,并对种族差异进行了讨论和评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f576/1685456/77d781dcd015/ajhg00199-0090-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f576/1685456/77d781dcd015/ajhg00199-0090-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f576/1685456/77d781dcd015/ajhg00199-0090-a.jpg

相似文献

1
Polymorphism of chromosome 9 in 600 Greek subjects.600名希腊受试者的9号染色体多态性
Am J Hum Genet. 1978 Jan;30(1):85-9.
2
Morphologic variability of human chromosomes: polymorphism of constitutive heterochromatin.人类染色体的形态变异:组成型异染色质的多态性
Hum Genet. 1976 May 19;32(2):149-54. doi: 10.1007/BF00291498.
3
Constitutive heterochromatin studies in patients with solid tumors.实体瘤患者的组成型异染色质研究。
J Cancer Res Clin Oncol. 1986;111(3):291-4. doi: 10.1007/BF00389248.
4
Structural organization of the heterochromatic region of human chromosome 9.人类9号染色体异染色质区域的结构组织
Chromosoma. 1981;84(3):353-63. doi: 10.1007/BF00286025.
5
C-band heteromorphism in breast cancer patients.乳腺癌患者的C波段异质性
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6
[Polymorphism of the heterochromatic regions of chromosomes 1, 9, 16 and Y and mental retardation].[1、9、16号染色体及Y染色体异染色质区多态性与智力发育迟缓]
Genetika. 1984 Jan;20(1):177-82.
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Satellite DNA and cytological staining patterns in heterochromatic inversions of human chromosome 9.人类9号染色体异染色质倒位中的卫星DNA和细胞学染色模式
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[Human chromosome polymorphism and disordered reproductive function. II. C-variant chromosomes].[人类染色体多态性与生殖功能紊乱。II. C变异染色体]
Genetika. 1979;15(10):1870-9.
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Chromosomal variability of sex chromosomes and NOR's in Trichomys apereoides (Rodentia, Echimyidae).绒毛鼠(啮齿目,棘鼠科)性染色体和核仁组织区的染色体变异性
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Heterochromatic polymorphism in spontaneous abortions.自然流产中的异染色质多态性。
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引用本文的文献

1
Chromosomal polymorphisms associated with reproductive outcomes after IVF-ET.与 IVF-ET 后生殖结局相关的染色体多态性。
J Assist Reprod Genet. 2020 Jul;37(7):1703-1710. doi: 10.1007/s10815-020-01793-8. Epub 2020 May 25.
2
Pericentric inversion of chromosome 9 in infertile men.不育男性的9号染色体臂间倒位
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3
Chromosomal anomalies in cryptorchidism.隐睾症中的染色体异常。

本文引用的文献

1
Chromosome polymorphism in American Negro and White populations.美国黑人和白人种群中的染色体多态性。
Nature. 1971 Sep 10;233(5315):134-6. doi: 10.1038/233134a0.
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Pericentric inversions of human chromosomes 9 and 10.人类9号和10号染色体的臂间倒位
Am J Hum Genet. 1974 Nov;26(6):746-66.
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Structural variation in chromosome No 9.9号染色体的结构变异
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Partial inversion of the secondary constriction of chromosome 9. Does it exist?9号染色体次缢痕的部分倒位。它存在吗?
Hum Genet. 1981;59(4):310-6. doi: 10.1007/BF00295463.
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Normal psychomotor development in a child with mosaic trisomy and pericentric inversion of chromosome 9.一名患有9号染色体嵌合三体和臂间倒位的儿童的正常精神运动发育。
J Med Genet. 1981 Oct;18(5):390-2. doi: 10.1136/jmg.18.5.390.
6
Structural organization of the heterochromatic region of human chromosome 9.人类9号染色体异染色质区域的结构组织
Chromosoma. 1981;84(3):353-63. doi: 10.1007/BF00286025.
7
Quantitative analysis of C bands in chromosomes 1, 9, and 16 of Brazilian Indians and Caucasoids.巴西印第安人和高加索人1号、9号及16号染色体C带的定量分析。
Hum Genet. 1981;57(1):58-63. doi: 10.1007/BF00271168.
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C heterochromatin variation in couples with recurrent early abortions.复发性早期流产夫妇中的C异染色质变异
J Med Genet. 1983 Oct;20(5):350-6. doi: 10.1136/jmg.20.5.350.
9
Chromosome anomalies in 136 couples with a history of recurrent abortions.136对有反复流产史夫妇的染色体异常情况。
Hum Genet. 1983;65(1):48-52. doi: 10.1007/BF00285027.
10
Probable linkage between the human galactose-1-P uridyl transferase locus and 9qh.人类1-磷酸半乳糖尿苷酰转移酶基因座与9号染色体长臂之间可能存在的连锁关系。
Am J Hum Genet. 1980 Mar;32(2):188-93.
Ann Genet. 1974 Jun;17(2):81-6.
4
Frequency of 9qh+ and risk of chromosome aberrations in the progeny of individuals with 9qh+.9qh+个体后代中9qh+的频率及染色体畸变风险。
Humangenetik. 1974;21(3):211-6. doi: 10.1007/BF00279014.
5
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.
6
Staining of some specific regions of human chromosomes, particularly the secondary constriction of No. 9.人类染色体某些特定区域的染色,尤其是9号染色体的次缢痕。
Nat New Biol. 1972 Jul 26;238(82):122-4. doi: 10.1038/newbio238122a0.
7
Morphologic variability of human chromosomes: polymorphism of constitutive heterochromatin.人类染色体的形态变异:组成型异染色质的多态性
Hum Genet. 1976 May 19;32(2):149-54. doi: 10.1007/BF00291498.
8
Chromosome polymorphism in a human newborn population. II. Potentials of polymorphic chromosome variants for characterizing the idiogram of an individual.人类新生儿群体中的染色体多态性。II. 多态性染色体变异体用于表征个体核型图的潜力。
Cytogenet Cell Genet. 1975;15(4):239-55. doi: 10.1159/000130522.
9
Association of pericentric inversion of chromosome 9 and reproductive failure in ten unrelated families.十个非亲缘家庭中9号染色体臂间倒位与生殖功能衰竭的关联
Humangenetik. 1975 Sep 20;30(3):217-24. doi: 10.1007/BF00279187.
10
Human Q and C chromosomal variations: distribution and incidence.人类Q和C染色体变异:分布与发生率
Cytogenet Cell Genet. 1975;14(2):97-115. doi: 10.1159/000130330.