Characterization and identification of Hb Bart’s hydrops fetalis caused by a compound heterozygous mutation ‐‐ SEA /‐‐ CR , a novel α 0 ‐thalassemia deletion-Reference-Cited by-同舟云学术

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

Published:2020-01-13 Issue:3 Volume:42 Page:
ISSN:1751-5521
Container-title:International Journal of Laboratory Hematology
language:en
Short-container-title:Int J Lab Hem

Author:

Ruengdit Chedtapak¹,Panyasai Sitthichai²,Kunyanone Naowarat³,Phornsiricharoenphant Worawich⁴,Ngamphiw Chumpol⁴,Tongsima Sissades⁴,Sripichai Orapan⁵,Pissard Serge⁶,Pornprasert Sakorn¹^ORCID

Affiliation:

1. Department of Medical Technology Faculty of Associated Medical Sciences Chiang Mai University Chiang Mai Thailand

2. School of Allied Health Sciences University of Phayao Phayao Thailand

3. Department of Medical Laboratory Chiang Rai Prachanukroh Hospital Chiang Rai Thailand

4. National Biobank of Thailand National Center for Genetic Engineering and Biotechnology National Science and Technology Development Agency Pathum Thani Thailand

5. Department of Medical Sciences Ministry of Public Health National Institute of Health Nonthaburi Thailand

6. Département de Génétique Hôpital Henri Mondor Assistance Publique‐Hôpitaux de Paris (APHP) Créteil France

Funder

Chiang Mai University

Publisher

Wiley

Subject

Biochemistry (medical),Clinical Biochemistry,Hematology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ijlh.13154

Reference12 articles.

1. α-thalassaemia

2. Hemoglobin H disease: not necessarily a benign disorder

3. Characterization of two deletions that remove the entire human ζ-α globin gene complex (—THAIand —FIL)

4. Molecular basis of alpha (0)‐thalassemia in northeast of Thailand;Fucharoen G;Southeast Asian J Trop Med Public Health,1995

5. The molecular basis of alpha-thalassaemia in Thailand.

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