المؤلفون: Licia Lugli, Fabrizio Ferrari, Agnese Marrone, Maria D'Apolito, Alberto Berardi, Achille Iolascon, Giancarlo Gargano

المساهمون: Berardi, A, Lugli, L, Ferrari, F, Gargano, G, D'Apolito, M, Marrone, A, Iolascon, Achille

مصطلحات موضوعية: Hemolytic anemia, Gilbert Syndrome, Male, medicine.medical_specialty, Pediatrics, Bilirubin, Spherocytosis, Spherocytosis, Hereditary, Biology, Hereditary spherocytosis, chemistry.chemical_compound, Internal medicine, kernicterus, medicine, Humans, Neonatology, Glucuronosyltransferase, Promoter Regions, Genetic, Kernicterus, Polymorphism, Genetic, Infant, Newborn, medicine.disease, Metabolism disorder, Pedigree, Endocrinology, chemistry, Hematocrit, NEAR-TERM INFANTS, GILBERTS-SYNDROME, (TA)(8) ALLELE, GENE PROMOTER, Pediatrics, Perinatology and Child Health, Developmental Biology

وصف الملف: ELETTRONICO

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef369472973ad28a7f39107da8c31598
http://hdl.handle.net/11588/472354