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Hinf I polymorphism 3' to the human beta-globin gene detected by the polymerase chain reaction (PCR).

作者信息

Semenza G L, Dowling C E, Kazazian H H

机构信息

Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD 21205.

出版信息

Nucleic Acids Res. 1989 Mar 25;17(6):2376. doi: 10.1093/nar/17.6.2376.

DOI:10.1093/nar/17.6.2376
PMID:2565032
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC317624/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f99/317624/2a442682eb93/nar00123-0222-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f99/317624/2a442682eb93/nar00123-0222-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f99/317624/2a442682eb93/nar00123-0222-a.jpg

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本文引用的文献

1
The mutation and polymorphism of the human beta-globin gene and its surrounding DNA.人类β-珠蛋白基因及其周围DNA的突变和多态性。
Annu Rev Genet. 1984;18:131-71. doi: 10.1146/annurev.ge.18.120184.001023.
通过高分辨率缺失图谱在人类非小细胞肺癌中鉴定出的11号染色体短臂上的三个肿瘤抑制区域。
Proc Natl Acad Sci U S A. 1994 Jun 7;91(12):5513-7. doi: 10.1073/pnas.91.12.5513.
4
Novel promoter and splice junction defects add to the genetic, clinical or geographic heterogeneity of beta-thalassaemia in the Portuguese population.新型启动子和剪接连接缺陷增加了葡萄牙人群中β地中海贫血的遗传、临床或地理异质性。
Hum Genet. 1992 Jul;89(5):573-6. doi: 10.1007/BF00219188.
5
A novel sickle cell mutation of yet another origin in Africa: the Cameroon type.非洲另一起源的新型镰状细胞突变：喀麦隆型。
Hum Genet. 1992 May;89(3):333-7. doi: 10.1007/BF00220553.
6
Analysis of beta-globin gene haplotypes in Asian Indians: origin and spread of beta-thalassaemia on the Indian subcontinent.亚洲印度人β-珠蛋白基因单倍型分析：β地中海贫血在印度次大陆的起源与传播
Hum Genet. 1992 Dec;90(4):443-9. doi: 10.1007/BF00220475.