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一种新的3.8 kb缺失α地贫基因的鉴定

OBJECTIVE: To report the identification of a novel 3.8-kb deletion that caused α thalassemia and establish the method for detecting the deletion fragment. METHODS: Peripheral blood samples were collected from the proband and his mother for analysis of the hematological parameters and routine test fo...

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Dades bibliogràfiques
Publicat a:Nan Fang Yi Ke Da Xue Xue Bao
Format: Artigo
Idioma:Inglês
Publicat: 南方医科大学学报编辑部 2017
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6765508/
https://ncbi.nlm.nih.gov/pubmed/28736383
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3969/j.issn.1673-4254.2017.07.26
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