Literature DB >> 26462784

[Molecular and prenatal diagnosis of a rare mutation IVS1-116（A→G）of α2-globin gene].

Danqing Qin1, Jicheng Wang1, Lihua Yu1, Tenglong Yuan1, Yanxia Zhang1, Yixia Wang1, Mingyong Luo1, Juqing Liang1, Li Du1.   

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Year:  2015        PMID： 26462784     DOI： 10.3760/cma.j.issn.0253-2727.2015.09.016

Source DB:  PubMed          Journal:  Zhonghua Xue Ye Xue Za Zhi        ISSN： 0253-2727


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  1 in total

1.  Compound heterozygosity for hemoglobin variant Hb-Broomhill and the Southeast Asian α-thalassemia deletion does not worsen outcome: a case report of two unrelated patients.

Authors:  Danqing Qin; Li Du; Jicheng Wang; Cuize Yao; Hao Guo; Tenglong Yuan; Jie Liang; Aihua Yin
Journal:  J Int Med Res       Date:  2020-11       Impact factor: 1.671
  1 in total

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