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Clinical study on the prevention of kernicterus caused by hereditary glucose-6-phosphate dehydrogenase deficiency
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Two commonly occurring nucleotide base substitutions in Chinese G6PD variants
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Six point mutations found in Chinese with glucose-6-phosphate dehydrogenase deficiency
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A novel point mutation in the G6PD gene among Chinese - An exon 6 cDNA 592C to T transition
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G6PD NanKang (517T→C; 173 Phe→Leu): A new Chinese G6PD variant associated with neonatal jaundice
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A case of 1004C→A gene mutation in Yunnan people
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Detection and clinical analysis of two mutations of glucose-6-phosphate dehydrogenase gene
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Gene mutations of glucose-6-phosphate dehydrogenase found in Qianxi, Guizhou
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The G6PD variants in a family of national minority Dai in Yunnan Province
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Molecular characterization of glucose-6-phosphate dehydrogenase (G6PD) deficiency by natural and amplification created restriction sites: Five mutations account for most G6PD deficiency cases in Taiwan
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Identification of G6PD gene mutations in several nationalities from Yunnan province
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A nitroblue tetrazolium paper strip method for screen G6PD deficiency
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An assay for red cell glucose-6-phosphate dehydrogenase deficiency by G6PD/ 6PGD ratio
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