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
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2020
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th-cmuir.6653943832-682752020-04-02T15:29:16Z 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 Biochemistry, Genetics and Molecular Biology Medicine 2020-04-02T15:24:07Z 2020-04-02T15:24:07Z 2020-01-01 Journal 1751553X 17515521 2-s2.0-85077975755 10.1111/ijlh.13154 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85077975755&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/68275 |
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Chiang Mai University |
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Chiang Mai University Library |
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Thailand |
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CMU Intellectual Repository |
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Biochemistry, Genetics and Molecular Biology Medicine |
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Biochemistry, Genetics and Molecular Biology Medicine Chedtapak Ruengdit Sitthichai Panyasai Naowarat Kunyanone Worawich Phornsiricharoenphant Chumpol Ngamphiw Sissades Tongsima Orapan Sripichai Serge Pissard Sakorn Pornprasert 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 |
format |
Journal |
author |
Chedtapak Ruengdit Sitthichai Panyasai Naowarat Kunyanone Worawich Phornsiricharoenphant Chumpol Ngamphiw Sissades Tongsima Orapan Sripichai Serge Pissard Sakorn Pornprasert |
author_facet |
Chedtapak Ruengdit Sitthichai Panyasai Naowarat Kunyanone Worawich Phornsiricharoenphant Chumpol Ngamphiw Sissades Tongsima Orapan Sripichai Serge Pissard Sakorn Pornprasert |
author_sort |
Chedtapak Ruengdit |
title |
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 |
title_short |
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 |
title_full |
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 |
title_fullStr |
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 |
title_full_unstemmed |
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 |
title_sort |
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 |
publishDate |
2020 |
url |
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85077975755&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/68275 |
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1681426790318342144 |