← Evidence map

ReviewTrends in genetics : TIG2022

Phenotype-aware prioritisation of rare Mendelian disease variants.

Catherine Kelly et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

26 papers cite it

2022
2023
2024
2025
2026
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 35934592