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2 ensaios clínicos encontrados.
Hereditary red cell defects as an underrecognized cause of neonatal jaundice.
Crossed Erythrocytes Agglutination Pattern Observed in a Patient With Hereditary Elliptocytosis.
A Male Child With Combined Glucose-6-Phosphate Dehydrogenase Deficiency and Hereditary Elliptocytosis: The First Case Reported From Saudi Arabia.
Hereditary elliptocytosis in a child with an autosomal recessive SPTA1 mutation: a case report from Saudi Arabia.
Frameshift Mutation in the EPB41 Gene with Hereditary Elliptocytosis.