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Heterozygous β‐thalassemia with complete absence of hemoglobin A 2 in a C hinese adult
Author(s) -
Yan J.M.,
Wu M.Y.,
Xie X.M.,
Li D.Z.
Publication year - 2015
Publication title -
international journal of laboratory hematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.705
H-Index - 55
eISSN - 1751-553X
pISSN - 1751-5521
DOI - 10.1111/ijlh.12396
Subject(s) - microcytosis , thalassemia , medicine , prenatal diagnosis , asymptomatic , genetic counseling , compound heterozygosity , fetal hemoglobin , beta thalassemia , hemoglobin a2 , pediatrics , anemia , fetus , genetics , pregnancy , biology , allele , iron deficiency , gene
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