Associated Papers
Whole genome sequencing reveals population diversity and variation in HIV-1 specific host genes.
Thami PK et al.
Frontiers in Genetics, 2023
38179408 (PubMed )
Supplement: Table6.XLSX › Table_S3
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 › HL3
Embryonic signature distinguishes pediatric and adult rhabdoid tumors from other SMARCB1-deficient cancers.
Richer W et al.
Oncotarget, 2017
28427232 (PubMed )
Supplement: oncotarget-08-34245-s004.xlsx › Sheet_1
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