Strong Linkage of the Single Nucleotide Polymorphism rs77308790 with an α0-Thalassemia (– –SEA deletion) Allele and Application for Double-Check Diagnosis of Hb Bart’s Hydrops Fetalis Syndrome in Thailand-Reference-Cited by-同舟云学术

Strong Linkage of the Single Nucleotide Polymorphism rs77308790 with an α0-Thalassemia (– –SEA deletion) Allele and Application for Double-Check Diagnosis of Hb Bart’s Hydrops Fetalis Syndrome in Thailand

Published:2019-09-03 Issue:4-5 Volume:43 Page:236-240
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Jomoui Wittaya¹^ORCID,Tepakhan Wanicha²,Karnpean Rossarin³

Affiliation:

1. Department of Pathology, Maha Chakri Sirindhorn Medical Center, Faculty of Medicine, Srinakharinwirot University, Nakhon Nayok, Thailand;

2. Department of Pathology, Faculty of Medicine, Prince of Songkla University, Songkhla, Thailand;

3. College of Medicine and Public Health, Ubon Ratchathani University, Ubon Ratchathani, Thailand

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2019.1666720

Reference18 articles.

1. THALASSEMIA IN THAILAND

2. 4 Pathophysiology of thalassaemia

3. α-Thalassemia: Hb H Disease and Hb Barts Hydrops Fetalis

4. Molecular prenatal diagnosis of alpha and beta thalassemia in pregnant Hakka women in southern China

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