← Evidence map

ArticleNature communications2022

Specialist multidisciplinary input maximises rare disease diagnoses from whole genome sequencing.

William L Macken et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

23 papers cite it

2022
2023
2024
2025
2026
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 36344503