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Hereditary erythrocyte enzymopathies in newborn infants with hyperbilirubinemia
Hereditary erythrocyte enzymopathies in newborn infants with hyperbilirubinemia
1985
Velázquez Al
Rico Ng
Ibarra B
Blancarte R
Cardosa J
Fonseca S
Maldonado E
Enríquez Ma
Medina C
Cantú Jm
Keywords:
Pyruvate kinase
Glucosephosphate Dehydrogenase Deficiency
infant newborn
Internal medicine
Endocrinology
Medicine
Correction
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