K. Sanpakit

Direct detection for G6PD Bangkok and G6PD Bangkok Noi mutations in the families with chronic nonspherocytic hemolytic anemia (CNSHA)

V. Tanphaichitr, W. Thongnoppakhun, A. Treesucon, 2015, International journal of laboratory hematology.

Inappropriate use of protein C, protein S, and antithrombin testing for hereditary thrombophilia screening: an experience from a large university hospital

Y. Nilanont, C. Wongwanit, P. Tientadakul, 2011, International journal of laboratory hematology.

Identification of mutations in the uroporphyrinogen III synthase gene in a Thai girl patient with congenital erythropoietic porphyria

V. Tanphaichitr, W. Thongnoppakhun, A. Treesucon, 2015, International journal of laboratory hematology.

Clinical Phenotypes and Molecular Diagnosis in a Hitherto Interaction of Hb E / β Thalassemia Syndrome ( β E / β-31 , A → G )

V. Viprakasit, G. Veerakul, V. Tanphaichitr, 2005 .