Identification of three different alpha-thalassemic haplotypes: -alpha 3.7, (--)MED and alpha Hph alpha in the same Algerian family.
作者信息
Leclerc T, Guetarni D, Bernet A, Colonna P, Godet J, Morlé F
机构信息
Centre de Génétique Moléculaire et Cellulaire, CNRS UMR106, Villeurbanne, France.
出版信息
Hum Mutat. 1995;5(2):182-3. doi: 10.1002/humu.1380050214.
PMID:7749418
Abstract
摘要
相似文献
1
Identification of three different alpha-thalassemic haplotypes: -alpha 3.7, (--)MED and alpha Hph alpha in the same Algerian family.
Hum Mutat. 1995;5(2):182-3. doi: 10.1002/humu.1380050214.
2
Molecular basis of alpha-thalassemia in Algeria.阿尔及利亚α地中海贫血的分子基础。
Hemoglobin. 2008;32(3):273-8. doi: 10.1080/03630260802004301.
3
Prenatal diagnosis of unusual hemoglobinopathies.
Am J Med Genet. 1994 Mar 1;50(1):15-20. doi: 10.1002/ajmg.1320500104.
4
[New contributions to the molecular study of alpha-thalassemia].[α地中海贫血分子研究的新贡献]
Rev Invest Clin. 1997 May;49 Suppl 1:6-7.
5
A new polymorphim (G->A) in the psizeta1 globin gene.
Haematologica. 2000 Sep;85(9):899-901.
6
Detection and haplotype differentiation of Southeast Asian alpha-thalassemia using polymerase chain reaction and a piezoelectric biosensor immobilized with a single oligonucleotide probe.利用聚合酶链反应和固定有单链寡核苷酸探针的压电生物传感器检测东南亚α-地中海贫血并进行单倍型区分
Transl Res. 2008 May;151(5):246-54. doi: 10.1016/j.trsl.2007.12.009. Epub 2008 Jan 28.
7
Nondeletional alpha-thalassemia: first description of alpha Hph alpha and alpha Nco alpha mutations in a Spanish population.
Am J Hematol. 1996 Jul;52(3):144-9. doi: 10.1002/(SICI)1096-8652(199607)52:3<144::AID-AJH3>3.0.CO;2-T.
8
Detection of alpha-globin gene disorders by a simple PCR methodology.通过一种简单的聚合酶链反应（PCR）方法检测α-珠蛋白基因疾病。
Haematologica. 1996 Sep-Oct;81(5):387-96.
9
10
Molecular analysis of Hb Q-H disease and Hb Q-Hb E in a Singaporean family.新加坡一个家庭中Hb Q-H病和Hb Q-Hb E的分子分析。
Southeast Asian J Trop Med Public Health. 1995;26 Suppl 1:252-6.
Zotero 插件