β-Globin chain abnormalities with coexisting α-thalassemia mutations.
about
KLF1 gene and borderline hemoglobin A2 in Saudi population.Laboratory parameters provided by Advia 2120 analyser identify structural haemoglobinopathy carriers and discriminate between Hb S trait and Hb C trait.Molecular spectrum of α-globin gene mutations in the Aegean region of Turkey: first observation of three α-globin gene mutations in the Turkish population.
P2860
β-Globin chain abnormalities with coexisting α-thalassemia mutations.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年学术文章
@wuu
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
@zh
2012年學術文章
@zh-hant
name
β-Globin chain abnormalities with coexisting α-thalassemia mutations.
@ast
β-Globin chain abnormalities with coexisting α-thalassemia mutations.
@en
type
label
β-Globin chain abnormalities with coexisting α-thalassemia mutations.
@ast
β-Globin chain abnormalities with coexisting α-thalassemia mutations.
@en
prefLabel
β-Globin chain abnormalities with coexisting α-thalassemia mutations.
@ast
β-Globin chain abnormalities with coexisting α-thalassemia mutations.
@en
P2093
P2860
P356
P1476
β-Globin chain abnormalities with coexisting α-thalassemia mutations.
@en
P2093
Abdullah Canataroglu
Birol Guvenc
Cagatay Unsal
Ferda Tekin Turhan
Hakan Erkman
Sevcan Tug Bozdogan
Sule Menziletoglu Yildiz
Suleyman Dincer
P2860
P304
P356
10.5114/AOMS.2012.28723
P577
2012-05-29T00:00:00Z