Associated Papers
A Novel Tool for the Analysis and Detection of Copy Number Variants Associated with Haemoglobinopathies.
Minaidou A et al.
International Journal of Molecular Sciences, 2022
36555557 (PubMed )
Supplement: ijms-23-15920-s001.zip › Supplementary_File_S1.xlsx › Sheet1
Clinical Genotyping by Next Generation Sequencing Reveals a Novel, De Novo β-Globin Gene Mutation Causing Hemolytic Anemia in a Chinese Individual.
Pu J et al.
Hemoglobin, 2018
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