Satellite associations of D group chromosomes in translocation carriers.
作者信息
Nakagome Y, Bloom A D
出版信息
J Med Genet. 1970 Dec;7(4):371-3. doi: 10.1136/jmg.7.4.371.
Abstract
摘要
相似文献
1
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
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Patterns of D chromosome involvement in human (DqDq) and (DqGq) Robertsonian rearrangements.人类（DqDq）和（DqGq）罗伯逊重排中D染色体的参与模式。
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Nonrandomness of translocations in man: preferential entry of chromosomes into 13-15-21 translocations.人类易位的非随机性：染色体优先进入13 - 15 - 21易位。
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DNA replication analysis of six 13-15--21 translocation families.六个13 - 15 - 21易位家族的DNA复制分析。
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Identification of the D chromosome with shortened long arm.具有缩短长臂的D染色体的鉴定。
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Presumptive C-15 translocation and familial large Y identified by autoradiography.通过放射自显影鉴定出推定的C-15易位和家族性大Y染色体。
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A partial D-trisomy-normal mosaic female.一名部分D三体-正常嵌合型女性。
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Smaller G (Gp-) and t (Gp-; Dp+) chromosomes. A familial study with one member having acute leukemia.
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引用本文的文献
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Possible origin of a small bisatellited additional chromosome.一条小的双随体额外染色体的可能起源。
Hum Genet. 1980;54(3):319-22. doi: 10.1007/BF00291576.
2
On the non-random involvement of D-group chromosomes in centric fusion translocations in man.
Humangenetik. 1971;11(4):351-4. doi: 10.1007/BF00278667.
3
Patterns of D chromosome involvement in human (DqDq) and (DqGq) Robertsonian rearrangements.人类（DqDq）和（DqGq）罗伯逊重排中D染色体的参与模式。
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Frequency of satellite association in individuals with structural abnormalities of nucleolus organiser region.核仁组织区结构异常个体中卫星联合的频率。
Humangenetik. 1973 Apr 16;18(2):111-5. doi: 10.1007/BF00291477.
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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。
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Inheritance of acrocentric association patterns.近端着丝粒联合模式的遗传
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Quantitative and qualitative study of acrocentric associations in 109 normal subjects.109名正常受试者近端着丝粒染色体联合的定量和定性研究。
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Distribution of human chromosomes on the metaphase plate using banding techniques.运用显带技术对中期板上人类染色体的分布情况进行研究。
Hum Genet. 1977 Nov 2;39(1):39-61. doi: 10.1007/BF00273152.
本文引用的文献
1
FAMILIAL D~D TRANSLOCATION. REPORT OF A PEDIGREE AND DNA REPLICATION ANALYSIS.家族性D~D易位。一个家系报告及DNA复制分析
N Engl J Med. 1964 Nov 26;271:1133-7. doi: 10.1056/NEJM196411262712203.
2
THE SITES OF NUCLEOLUS FORMATION IN HUMAN PACHYTENE CHROMOSOMES.人类粗线期染色体上核仁形成的位点
Cytogenetics. 1964;3:124-34. doi: 10.1159/000129803.
3
Nucleolus-organisers in the causation of chromosomal anomalies in man.人类染色体异常病因中的核仁组织者
Lancet. 1961 Jul 15;2(7194):123-6. doi: 10.1016/s0140-6736(61)92647-2.
4
Observations on the satellited human chromosomes.关于人类随体染色体的观察
Lancet. 1961 Mar 25;1(7178):638-40. doi: 10.1016/s0140-6736(61)91655-5.
5
Identification of translocated chromosomes by means of autoradiography.通过放射自显影术鉴定易位染色体。
Paediatr Univ Tokyo. 1967 Jun;14:14-20.
6
Satellite association (SA) in familial mosaicism.家族性镶嵌现象中的卫星体联合（SA）
Helv Paediatr Acta. 1966 Sep;21(4):293-9.
7
Transmission of a D/D reciprocal translocation in a family with high incidence of mental retardation.一个智力发育迟缓高发家族中D/D相互易位的传递
Am J Hum Genet. 1966 May;18(3):288-95.
8
The identification of the chromosomes of the D group (13-15) Denver: an autoradiographic and measurement study.D组（13 - 15）染色体的鉴定：一项放射自显影及测量研究。 丹佛
Cytogenetics. 1966;5(3):186-205. doi: 10.1159/000129897.
9
Translocation between both members of chromosome pair number 15 causing recurrent abortions.15号染色体对的两个成员之间发生易位，导致反复流产。
Ann Hum Genet. 1969 May;32(4):347-52. doi: 10.1111/j.1469-1809.1969.tb00085.x.
10
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.
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