← Evidence map

ArticleEuropean journal of human genetics : EJHG2021

Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data.

Leslie Matalonga et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

Not cited yet

Full record →Abstract, authors, funding and every citing paper · PMID 34393220