Characterization of alpha thalassemic genotypes by multiplex ligation-dependent probe amplification in the Brazilian population.
about
Rare α0-thalassemia deletions detected by MLPA in five unrelated Brazilian patients.Detection of α-Thalassemia by Using Multiplex Ligation-Dependent Probe Amplification as an Additional Method for Rare Mutations in Southern Turkey.Two novel copy number variations involving the α-globin gene cluster on chromosome 16 cause thalassemia in two Chinese families.Novel 31.2 kb α0 Deletion in a Palestinian Family with α-Thalassemia.
P2860
Characterization of alpha thalassemic genotypes by multiplex ligation-dependent probe amplification in the Brazilian population.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
2010年學術文章
@zh
2010年學術文章
@zh-hant
name
Characterization of alpha thal ...... n in the Brazilian population.
@en
Characterization of alpha thal ...... n in the Brazilian population.
@nl
type
label
Characterization of alpha thal ...... n in the Brazilian population.
@en
Characterization of alpha thal ...... n in the Brazilian population.
@nl
prefLabel
Characterization of alpha thal ...... n in the Brazilian population.
@en
Characterization of alpha thal ...... n in the Brazilian population.
@nl
P2093
P2860
P1476
Characterization of alpha thal ...... n in the Brazilian population.
@en
P2093
A S Araújo
C N Suemasu
D M Oliveira
E M Kimura
M A C Bezerra
M F Sonati
P2860
P356
10.1590/S0100-879X2010007500144
P407
P577
2010-12-17T00:00:00Z