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Characterization and identification of Hb Bart’s hydrops fetalis caused by a compound heterozygous mutation ‐‐ SEA /‐‐ CR , a novel α 0 ‐thalassemia deletion
Author(s) -
Ruengdit Chedtapak,
Panyasai Sitthichai,
Kunya Naowarat,
Phornsiricharoenphant Worawich,
Ngamphiw Chumpol,
Tongsima Sissades,
Sripichai Orapan,
Pissard Serge,
Pornprasert Sakorn
Publication year - 2020
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.13154
Subject(s) - biobank , medicine , christian ministry , family medicine , agency (philosophy) , library science , thalassemia , hydrops fetalis , political science , genetics , law , biology , sociology , computer science , pregnancy , social science , gestation