The importance of being a fragile site.
作者信息
Hecht F, Kaiser-McCaw B
出版信息
Am J Hum Genet. 1979 Mar;31(2):223-5.
Abstract
摘要
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Heritable fragile sites and lymphocyte culture medium containing BrdU.可遗传的脆性位点和含有溴脱氧尿苷的淋巴细胞培养基。
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Inducing fragile sites to express themselves.诱导脆性位点表达自身。
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Fragile (X)(q27) sites in a pedigree with female carriers showing mild to severe mental retardation.一个家系中存在脆性（X）（q27）位点，家系中的女性携带者表现出轻度至重度智力发育迟缓。
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本文引用的文献
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Compound lateral asymmetry in human chromosome 6:BrdU-dye studies of 6q12-->6q14.人类6号染色体的复合性侧向不对称性：6q12→6q14的BrdU-染料研究
Am J Hum Genet. 1978 Mar;30(2):153-9.
2
Persisting clone of cells with an abnormal chromosome in a woman previously irradiated.在一名曾接受过辐射的女性体内持续存在的带有异常染色体的细胞克隆。
J Nucl Med. 1965 Oct;6(10):740-6.
3
A marker X chromosome.一条标记性X染色体。
Am J Hum Genet. 1969 May;21(3):231-44.
4
Heritable fragile site on chromosome 16: probable localization of haptoglobin locus in man.16号染色体上的遗传性脆性位点：人触珠蛋白基因座的可能定位。
Science. 1970 Oct 2;170(3953):85-7. doi: 10.1126/science.170.3953.85.
5
Constitutional chromosomal breakage.
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6
Fragile sites on human chromosomes: demonstration of their dependence on the type of tissue culture medium.人类染色体上的脆性位点：其对组织培养基类型依赖性的证明
Science. 1977 Jul 15;197(4300):265-6. doi: 10.1126/science.877551.
7
Familial X-linked mental retardation with an X chromosome abnormality.
J Med Genet. 1977 Feb;14(1):46-50. doi: 10.1136/jmg.14.1.46.
8
Giemsa-11 staining of chromosome 1: a newly described heteromorphism.
Science. 1978 Oct 6;202(4363):64-5. doi: 10.1126/science.694520.
9
Lateral asymmetry in human constitutive heterochromatin: frequency and inheritance.人类组成型异染色质的侧向不对称性：频率与遗传
Am J Hum Genet. 1978 Mar;30(2):144-52.
10
Heritable fragile sites on human chromosomes II. Distribution, phenotypic effects, and cytogenetics.人类染色体上的遗传性脆性位点II。分布、表型效应及细胞遗传学
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