Associated Papers
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Bmc Medical Genomics, 2020
32948195 (PubMed )
Supplement: 12920_2020_763_MOESM1_ESM.xls › Pat6
Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families.
Zhou Y et al.
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Supplement: 12881_2020_1087_MOESM1_ESM.xlsx › HL3
XomAnnotate: Analysis of Heterogeneous and Complex Exome- A Step towards Translational Medicine.
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25905921 (PubMed )
Supplement: pone.0123569.s008.xls › BC11_ERR166336
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