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Literature DB >> 26957072

[Screening and molecular diagnosis for a rare genotype of beta-thalassemia intermedia].

Jianhong Xie, Yuqiu Zhou, Qizhi Xiao.

Abstract

Entities: Disease

Mesh：

Year: 2016 PMID： 26957072 DOI： 10.3760/cma.j.issn.0578-1310.2016.03.015

Source DB: PubMed Journal: Zhonghua Er Ke Za Zhi ISSN： 0578-1310

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Cited

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2 in total

1. Molecular prenatal diagnosis of alpha and beta thalassemia in pregnant Hakka women in southern China.

Authors: Pingsen Zhao; Heming Wu; Zhixiong Zhong; Liubing Lan; Mei Zeng; Hualan Lin; Huaxian Wang; Zhiyuan Zheng; Luxian Su; Wei Guo
Journal: J Clin Lab Anal Date: 2017-08-03 Impact factor: 2.352

2. Prenatal diagnosis of a rare β-thalassemia gene －90 (C>T) (HBB: c.-140 C>T) mutation associated with deletional Hb H disease (--^SEA /-α^4.2 ).

Authors: Hou Qian; Jianlin Huang; Ji Xu; Weihua Zhao; Xiufeng Ye; Wenlan Liu
Journal: Mol Genet Genomic Med Date: 2020-09-03 Impact factor: 2.183

2 in total

[Screening and molecular diagnosis for a rare genotype of beta-thalassemia intermedia].

1. Molecular prenatal diagnosis of alpha and beta thalassemia in pregnant Hakka women in southern China.

2. Prenatal diagnosis of a rare β-thalassemia gene －90 (C>T) (HBB: c.-140 C>T) mutation associated with deletional Hb H disease (--SEA /-α4.2 ).

2. Prenatal diagnosis of a rare β-thalassemia gene －90 (C>T) (HBB: c.-140 C>T) mutation associated with deletional Hb H disease (--^SEA /-α^4.2 ).