Associated Papers
Precise diagnosis of a hereditary spherocytosis patient with complicated hematological phenotype.
Liang G et al.
Molecular Genetics and Genomics : Mgg, 2024
Whole-exome sequencing for the genetic diagnosis of congenital red blood cell membrane disorders in Taiwan.
Lin PC et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2018
Select a paper to view details