Associated Papers
Integrated Whole-Exome and Transcriptome Sequencing of Sporadic Parathyroid Adenoma.
Hu Y et al.
Frontiers in Endocrinology, 2021
34054720 (PubMed )
Supplement: Table_1.xlsx › Sheet1
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 › HL4
SF3B1 mutant MDS-initiating cells may arise from the haematopoietic stem cell compartment.
Mian SA et al.
Nature Communications, 2015
26643973 (PubMed )
Supplement: ncomms10004-s1.pdf
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