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阿拉巴马州黑人的囊性纤维化DNA标记

Cystic fibrosis DNA markers in Alabama blacks.

作者信息

Martin R K, Kaplan G C, Hodge T W, Barker P E

机构信息

Laboratory of Medical Genetics, University of Alabama, Birmingham 35294.

出版信息

Genomics. 1988 Nov;3(4):385-8. doi: 10.1016/0888-7543(88)90132-2.

DOI:10.1016/0888-7543(88)90132-2
PMID:3243554
Abstract

DNA samples from unrelated Alabama blacks with no family history of cystic fibrosis (CF) were analyzed with DNA markers linked to cf. Allelic frequencies of genetic markers detected by probes pmetH, pmetD, XV2c, KM19, and pJ3.11 were compared to those of other populations. Allelic frequencies for pJ3.11, XV2c, and KM19 in Alabama blacks and previously studied Caucasian populations were similar. In contrast, the met locus allelic frequencies in Alabama blacks were markedly different from those in Caucasian populations.

摘要

对来自阿拉巴马州、无囊性纤维化(CF)家族病史的非亲属黑人的DNA样本,使用与CF相关的DNA标记进行分析。将探针pmetH、pmetD、XV2c、KM19和pJ3.11检测到的遗传标记的等位基因频率与其他人群的进行比较。阿拉巴马州黑人中pJ3.11、XV2c和KM19的等位基因频率与之前研究的白种人群体相似。相比之下,阿拉巴马州黑人中met位点的等位基因频率与白种人群体明显不同。

相似文献

1
Cystic fibrosis DNA markers in Alabama blacks.阿拉巴马州黑人的囊性纤维化DNA标记
Genomics. 1988 Nov;3(4):385-8. doi: 10.1016/0888-7543(88)90132-2.
2
Analysis of DNA polymorphism haplotypes linked to the cystic fibrosis locus in North American black and Caucasian families supports the existence of multiple mutations of the cystic fibrosis gene.对北美黑人和白人家庭中与囊性纤维化基因座相关的DNA多态性单倍型的分析支持囊性纤维化基因存在多种突变。
Am J Hum Genet. 1989 Mar;44(3):307-18.
3
Cystic fibrosis: typing 89 German families with linked DNA probes.
Hum Genet. 1988 Dec;81(1):54-6. doi: 10.1007/BF00283729.
4
Further data supporting linkage between cystic fibrosis and the met oncogene and haplotype analysis with met and pJ3.11.支持囊性纤维化与met癌基因之间联系的进一步数据以及met和pJ3.11的单倍型分析。
Am J Hum Genet. 1986 Dec;39(6):713-9.
5
Analysis of four diverse population groups indicates that a subset of cystic fibrosis mutations occur in common among Caucasians.对四个不同人群组的分析表明,一部分囊性纤维化突变在白种人中普遍存在。
Am J Hum Genet. 1992 Jun;50(6):1185-94.
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DNA markers near the cystic fibrosis locus: further analysis of the British population.囊性纤维化基因座附近的DNA标记:对英国人群的进一步分析。
J Med Genet. 1990 Jan;27(1):39-41. doi: 10.1136/jmg.27.1.39.
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Allelic association of the cystic fibrosis locus and two DNA markers, XV2c and KM19, in 55 German families.55个德国家庭中囊性纤维化基因座与两个DNA标记XV2c和KM19的等位基因关联。
Hum Genet. 1988 Sep;80(1):78-80. doi: 10.1007/BF00451461.
8
Linkage of DNA markers to cystic fibrosis in 26 families.26个家族中DNA标记与囊性纤维化的连锁关系。
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D1S80 population data in African Americans, Caucasians, southeastern Hispanics, southwestern Hispanics, and Orientals.
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Transferrin receptor-2 (TFR2) mutation Y250X in Alabama Caucasian and African American subjects with and without primary iron overload.阿拉巴马州有和没有原发性铁过载的白种人和非裔美国受试者中,转铁蛋白受体2(TFR2)突变Y250X的情况
Blood Cells Mol Dis. 2001 Jan-Feb;27(1):279-84. doi: 10.1006/bcmd.2001.0380.

引用本文的文献

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Cystic fibrosis in Afro-Brazilians: XK haplotypes analysis supports the European origin of p.F508del mutation.非洲裔巴西人中的囊性纤维化:XK单倍型分析支持p.F508del突变的欧洲起源。
Genetica. 2017 Feb;145(1):19-25. doi: 10.1007/s10709-016-9942-x. Epub 2017 Feb 3.
2
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