在一种胎儿血红蛋白遗传性持续存在形式中，一个基因缺失终止于重复DNA序列的中点。 - Suppr

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超能文献

A gene deletion ending at the midpoint of a repetitive DNA sequence in one form of hereditary persistence of fetal haemoglobin.

作者信息

Jagadeeswaran P, Tuan D, Forget B G, Weissman S M

出版信息

Nature. 1982 Apr 1;296(5856):469-70. doi: 10.1038/296469a0.

DOI:10.1038/296469a0

PMID:6174873

Abstract

摘要

相似文献

A gene deletion ending at the midpoint of a repetitive DNA sequence in one form of hereditary persistence of fetal haemoglobin.在一种胎儿血红蛋白遗传性持续存在形式中，一个基因缺失终止于重复DNA序列的中点。

Nature. 1982 Apr 1;296(5856):469-70. doi: 10.1038/296469a0.

A gene deletion ending within a complex array of repeated sequences 3' to the human beta-globin gene cluster.一个在人类β-珠蛋白基因簇3'端的复杂重复序列阵列内结束的基因缺失。

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Heterogeneity of molecular defects underlying hereditary persistence of fetal hemoglobin in Mediterranean area.

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Hereditary persistence of fetal haemoglobin (HPFH) and delta beta thalassaemia.胎儿血红蛋白遗传性持续存在（HPFH）与δβ地中海贫血

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delta beta-Thalassemia and HPFH.δβ地中海贫血和遗传性胎儿血红蛋白持续增多症

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The sequence of the A gamma globin gene in a G gamma beta+ type of hereditary persistence of fetal haemoglobin.胎儿血红蛋白遗传性持续存在的Gγβ+型中Aγ珠蛋白基因的序列。

Br J Haematol. 1985 Feb;59(2):357-62. doi: 10.1111/j.1365-2141.1985.tb03000.x.

Compound heterozygosity of non-deletional hereditary persistence of fetal hemoglobin and deltabeta-thalassemia.非缺失型胎儿血红蛋白遗传性持续存在与δβ地中海贫血的复合杂合性

Am J Hematol. 2008 Sep;83(9):760. doi: 10.1002/ajh.21243.

Delta beta thalassemia and hereditary persistence of fetal hemoglobin.δ地中海贫血与胎儿血红蛋白遗传性持续存在

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Molecular comparison of delta beta-thalassemia and hereditary persistence of fetal hemoglobin DNAs: evidence of a regulatory area?δβ地中海贫血与胎儿血红蛋白DNA遗传性持续存在的分子比较：调控区域的证据？

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Am J Hum Genet. 1983 May;35(3):333-61.

Developmental fate of a human insulin gene in a transgenic mouse.人类胰岛素基因在转基因小鼠中的发育命运

Mol Gen Genet. 1984;198(2):128-38. doi: 10.1007/BF00328712.

The beta-globin gene in Sardinian delta beta 0-thalassemia carries a C----T nonsense mutation at codon 39.撒丁岛δβ0地中海贫血中的β-珠蛋白基因在第39密码子处存在一个C→T无义突变。

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