Associated Papers
Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families.
Zhou Y et al.
Bmc Medical Genetics, 2020
32682410 (PubMed )
Supplement: 12881_2020_1087_MOESM1_ESM.xlsx › HL1
Undifferentiated small round cell sarcoma in a young male: a case report.
Ricker CA et al.
Cold Spring Harbor Molecular Case Studies, 2020
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