Hemoglobin H disease induced by the common SEA deletion and the rare hemoglobin Quong Sze in a Thai female: longitudinal clinical course, molecular characterization, and development of a PCR/RFLP-based detection method

Author:

Sura Thanyachai,Trachoo Objoon,Viprakasit Vip,Vathesatogkit Prin,Tunteeratum Atchara,Busabaratana Manisa,Wisedpanichkij Raewadee,Isarangkura Parttraporn

Publisher

Springer Science and Business Media LLC

Subject

Hematology,General Medicine

Reference21 articles.

1. Weatherall DJ (2001) The Thalassemias. In: Stamatoyannopoulos G, Majerus PW, Perlmutter RM, Varmus H (eds) The molecular basis of blood diseases. Saunders, Pennsylvania, pp 183–226

2. Chui DHK, Fucharoen S, Chan V (2003) Hemoglobin H disease: not necessarily a benign disorder. Blood 101:791–800

3. Tangvarasittichai O, Jeenapomgsa R, Sitthiworanan C, Sanguansermsri T (2005) Laboratory investigations of Hb Constant Spring. Clin Lab Haematol 27:47–49

4. Harteveld CL, Traeger-Synodinos J, Ragusa A, Fichera M, Kanavakis E, Kattamis C, Giordano P, Schiliro G, Bernini LF (2001) Different geographic origins of Hb Constant Spring [α2 codon 142 TAA→CAA]. Haematologica 86:36–38

5. Viprakasit V, Tanphaichitr VS, Pung-Amritt P, Petrarat S, Suwantol L, Fisher C, Higgs DR (2002) Clinical phenotypes and molecular characterization of Hb H-Paksě disease. Haematologica 87:117–125

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