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Fig. 2 | BMC Pediatrics

Fig. 2

From: Co-inheritance of G6PD deficiency and 211 G to a variation of UGT1A1 in neonates with hyperbilirubinemia in eastern Guangdong

Fig. 2

A The location of the probes dotted in the gene chip used for the flow-through hybridization. Location of wild-type was denoted as N. Location of mutant probes was denoted as M. B Part of hybridization results of G6PD gene chip. 95 M, 392 M, 487 M, 1311 M, 1376 M, 1388 M, 1024 M, 95 M/1388 M, and 871 M/1311 M were positive on the G6PD gene chip

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BMC Pediatrics

ISSN: 1471-2431

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