Diagnosis of the clinical polymorphism of glucose-6-phosphate dehydrogenase deficiency in patients with hyperbilirubinemia
Two Azerbaijani families were examined to determine the nature of neonatal hyperbilirubinemia. Blood samples from neonatal infants with jaundice, their siblings, and parents were an object of this investigation. The pedigrees of the probands were compiled and analyzed. The levels of hemoglobin, red...
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| Format: | Article |
| Language: | Russian |
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Ltd. “The National Academy of Pediatric Science and Innovation”
2016-03-01
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| Series: | Rossijskij Vestnik Perinatologii i Pediatrii |
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| Online Access: | https://www.ped-perinatology.ru/jour/article/view/194 |