Associated Papers
Phenotypic and genotypic spectrum of noonan syndrome: A retrospective analysis of 46 consecutive pediatric patients presented at a regional cardiac center in China.
Chen Q et al.
Heliyon, 2024
38463782 (PubMed )
Supplement: mmc1.pdf
Cardiovascular Abnormalities and Gene Mutations in Children With Noonan Syndrome.
Sun L et al.
Frontiers in Genetics, 2022
The genomic and epigenomic evolutionary history of papillary renal cell carcinomas.
Zhu B et al.
Nature Communications, 2020
32555180 (PubMed )
Supplement: 41467_2020_16546_MOESM7_ESM.xlsx › Data_S4
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