Associated Papers
Congenital dyserythropoiesis anemia type Ia with a novel CDAN1 mutation diagnosed by whole exome sequencing.
Lin PC et al.
Molecular Genetics & Genomic Medicine, 2020
32160409 (PubMed )
Supplement: MGG3-8-e1220-s001.xlsx › ___1
Tumor heterogeneity and acquired drug resistance in FGFR2-fusion-positive cholangiocarcinoma through rapid research autopsy.
Krook MA et al.
Cold Spring Harbor Molecular Case Studies, 2019
31371345 (PubMed )
Supplement: supp_mcs.a004002_Supplemental_S1.xlsx › Left_kidney_lymph_node
Human primary liver cancer-derived organoid cultures for disease modeling and drug screening.
Broutier L et al.
Nature Medicine, 2017
29131160 (PubMed )
Supplement: NIHMS74480-supplement-Supplementary_Dataset_4.xlsx › S13_CC-3_coding_SNVs
Simultaneous evolutionary expansion and constraint of genomic heterogeneity in multifocal lung cancer.
Ma P et al.
Nature Communications, 2017
29018192 (PubMed )
Supplement: 41467_2017_963_MOESM2_ESM.xlsx › Supplementary_Data_1
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