Associated Papers
Pathologic Genetic Mutations May Correlate with Poor Visual Outcome in Patients with Hydroxychloroquine Retinopathy.
Chiu HI et al.
Ophthalmology and Therapy, 2025
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
Candidate genes for hereditary colorectal cancer: Mutational screening and systematic review.
Belhadj S et al.
Human Mutation, 2020
Updates in the field of hereditary nonpolyposis colorectal cancer.
Peltomäki P et al.
Expert Review of Gastroenterology & Hepatology, 2020
Whole-exome sequencing identifies a novel homozygous frameshift mutation in the PROM1 gene as a causative mutation in two patients with sporadic retinitis pigmentosa.
Liu S et al.
International Journal of Molecular Medicine, 2016
Molecular approach to genetic and epigenetic pathogenesis of early-onset colorectal cancer.
Tezcan G et al.
World Journal of Gastrointestinal Oncology, 2016
Germline variants in the SEMA4A gene predispose to familial colorectal cancer type X.
Schulz E et al.
Nature Communications, 2014
Familial Colorectal Cancer Type X (FCCTX) and the correlation with various genes-A systematic review.
Nejadtaghi M et al.
Current Problems in Cancer, 0
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