← Evidence map

ArticleHuman genetics2021

Systematic identification of genetic systems associated with phenotypes in patients with rare genomic copy number variations.

F M Jabato et al.PubMed ↗Publisher ↗

No numbers read from the abstract.

8 papers cite it

2021
2022
2023
2024
2025
2026
this papertrialcites it
Full record →Abstract, authors, funding and every citing paper · PMID 32778951