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1. Relationship between molecular variants and clinical manifestions in twelve glucose-6-phosphate dehydrogenase-deficient patients in Jordan.

Author

Karadsheh NS, Gelbart T, Schulten HJ, Efferth T, and Awidi A

Subjects
Anemia genetics, Favism genetics, Female, Humans, Infant, Newborn, Jaundice, Neonatal genetics, Jordan, Male, Anemia pathology, Favism pathology, Glucosephosphate Dehydrogenase genetics, Jaundice, Neonatal pathology, Point Mutation genetics
Published
2005
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