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Issue Date
Title
Author(s)
1-Jan-2020
Characterization and identification of Hb Bart’s hydrops fetalis caused by a compound heterozygous mutation --<sup>SEA</sup>/--<sup>CR</sup>, a novel α<sup>0</sup>-thalassemia deletion
Chedtapak Ruengdit
;
Sitthichai Panyasai
;
Naowarat Kunyanone
;
Worawich Phornsiricharoenphant
;
Chumpol Ngamphiw
;
Sissades Tongsima
;
Orapan Sripichai
;
Serge Pissard
;
Sakorn Pornprasert
3-Mar-2020
Proficiency Testing Program for Hb E (HBB: c.79G>A) Screening in Thailand Using Lyophilized Hb E Control Materials
Sakorn Pornprasert
;
Sirithorn Surajinda
;
Panida Pongpunyayuen
;
Manoo Punyamung
;
Chedtapak Ruengdit
;
Nutjeera Intasai
1-Jan-2020
Stability of control materials for α-thalassemia immunochromatographic strip test
Paweena Yanpanya
;
Chedtapak Ruengdit
;
Panida Pongpunyayuen
;
Sakorn Pornprasert
1-Jan-2022
Multiplex Quantitative Real-Time Polymerase Chain Reaction and High-Resolution Melting Analysis for Identification of a Couple At-Risk of Having a Newborn with Severe Thalassemia
Chedtapak Ruengdit
;
Manoo Punyamung
;
Pinyaphat Khamphikham
;
Panida Pongpunyayuen
;
Nutjeera Intasai
;
Sakorn Pornprasert
1-Jan-2021
Hb Bart’s Hydrops Fetalis Syndrome and Hb H Disease Caused by Deletional Chiang Rai (– –<sup>CR</sup>) α<sup>0</sup>-Thalassemia in Two Unrelated Thai Families
Chedtapak Ruengdit
;
Pinyaphat Khamphikham
;
Nathawat Jinorose
;
Sakorn Pornprasert
Discover
Author
1
Paweena Yanpanya
1
Serge Pissard
1
Sirithorn Surajinda
1
Sissades Tongsima
1
Sitthichai Panyasai
1
Worawich Phornsiricharoenphant
.
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