Associated Papers
Identification of a novel TOP2B::AFF2 fusion gene in B-cell acute lymphoblastic leukemia.
Liu T et al.
Scientific Reports, 2025
39863655 (PubMed )
Supplement: 41598_2025_86865_MOESM2_ESM.pdf
Novel mutations of the USH2A gene cause Usher syndrome in five Chinese families.
Xing D et al.
Bmc Ophthalmology, 2022
35870892 (PubMed )
Supplement: 12886_2022_2532_MOESM5_ESM.xlsx › Sheet1
The ChinaMAP analytics of deep whole genome sequences in 10,588 individuals.
Cao Y et al.
Cell Research, 2020
32355288 (PubMed )
Supplement: 41422_2020_322_MOESM14_ESM.xlsx › S7
Clinical and genetic study of 12 Chinese Han families with nonsyndromic deafness.
Wu D et al.
Molecular Genetics & Genomic Medicine, 2020
32048449 (PubMed )
Supplement: MGG3-8-e1177-s002.pdf
Genetic Analysis and Follow-Up of 25 Neonatal Diabetes Mellitus Patients in China.
Cao B et al.
Journal of Diabetes Research, 2016
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