Associated Papers
Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families.
Zhou Y et al.
Bmc Medical Genetics, 2020
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Supplement: 12881_2020_1087_MOESM1_ESM.xlsx › HL2
Single-cell analysis based dissection of clonality in myelofibrosis.
Mylonas E et al.
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Supplement: 41467_2019_13892_MOESM4_ESM.xlsx › MPN17
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