Search Results - Juntharaniyom, Monthana

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  1. 1
    Mutations in Krüppel-like factor 1 cause transfusion-dependent hemolytic anemia and persistence of embryonic globin gene expression

    Mutations in Krüppel-like factor 1 cause transfusion-dependent hemolytic anemia and persistence of embryonic globin gene expression by Viprakasit, Vip, Ekwattanakit, Supachai, Riolueang, Suchada, Chalaow, Nipon, Fisher, Chris, Lower, Karen, Kanno, Hitoshi, Tachavanich, Kalaya, Bejrachandra, Sasithorn, Saipin, Jariya, Juntharaniyom, Monthana, Sanpakit, Kleebsabai, Tanphaichitr, Voravarn S., Songdej, Duantida, Babbs, Christian, Gibbons, Richard J., Philipsen, Sjaak, Higgs, Douglas R.

    Published in Blood
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  2. 2
    Severe neonatal haemolytic anaemia caused by compound heterozygous KLF1 mutations: report of four families and literature review

    Severe neonatal haemolytic anaemia caused by compound heterozygous KLF1 mutations: report of four families and literature review by Tangsricharoen, Tanu, Natesirinilkul, Rungrote, Phusua, Arunee, Fanhchaksai, Kanda, Ittiwut, Chupong, Chetruengchai, Wanna, Juntharaniyom, Monthana, Charoenkwan, Pimlak, Viprakasit, Vip, Phokaew, Chureerat, Shotelersuk, Vorasuk

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