Search Results - "Glomglao, W"

Identification of mutations in the uroporphyrinogen III synthase gene in a Thai girl patient with congenital erythropoietic porphyria by Glomglao, W., Treesucon, A., Roothumnong, E., Thongnoppakhun, W., Siraprapapat, P., Suwanthol, L., Sanpakit, K., Tanphaichitr, V. S.

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Direct detection for G6PD Bangkok and G6PD Bangkok Noi mutations in the families with chronic nonspherocytic hemolytic anemia (CNSHA) by Glomglao, W., Chansing, K., Treesucon, A., Siraprapapat, P., Thongnoppakhun, W., Sanpakit, K., Tanphaichitr, V. S.

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Prevalence of HB E from cord blood samples and after one year follow-up by Pung-amritt, P, Tanphaichitr, V S, Tachavanich, K, Suwantol, L, Glomglao, W

“…Hemoglobin (Hb) E is the most prevalent hemoglobinopathy in Southeast Asia. The prevalence of this condition varies from 9-60% of the population in different…”
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Identification of mutations in the uroporphyrinogen III synthase gene in a Thai girl patient with congenital erythropoietic porphyria by Glomglao, W, Treesucon, A, Roothumnong, E, Thongnoppakhun, W, Siraprapapat, P, Suwanthol, L, Sanpakit, K, Tanphaichitr, V S

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