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Your search keyword '"Sripichai, Orapan"' showing total 4 results
Start Over Author "Sripichai, Orapan" Journal international journal of laboratory hematology
4 results on '"Sripichai, Orapan"'

2. Characterization and identification of Hb Bart’s hydrops fetalis caused by a compound heterozygous mutation ‐‐ SEA /‐‐ CR , a novel α 0 ‐thalassemia deletion

Author

Ruengdit, Chedtapak, primary, Panyasai, Sitthichai, additional, Kunyanone, Naowarat, additional, Phornsiricharoenphant, Worawich, additional, Ngamphiw, Chumpol, additional, Tongsima, Sissades, additional, Sripichai, Orapan, additional, Pissard, Serge, additional, and Pornprasert, Sakorn, additional

Published
2020
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4. Characterization and identification of Hb Bart's hydrops fetalis caused by a compound heterozygous mutation ‐‐SEA/‐‐CR, a novel α0‐thalassemia deletion.

Author

Ruengdit, Chedtapak, Panyasai, Sitthichai, Kunyanone, Naowarat, Phornsiricharoenphant, Worawich, Ngamphiw, Chumpol, Tongsima, Sissades, Sripichai, Orapan, Pissard, Serge, and Pornprasert, Sakorn

Subjects
CHROMOSOME abnormalities, GENE expression, GENETIC mutation, THALASSEMIA
Abstract

The article offers information on the characterization and identification of hemoglobin (Hb) Bart's hydrops fetalis caused by a compound heterozygous mutation. It discusses the Alpha thalassemia as one of the most common inherited hemoglobin (Hb) disorders, characterized by reduction or absence of the α-globin chain synthesis due to deletion or mutation of alpha-globin gene.

Published
2020
Full Text
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