← Evidence map

ArticleAnnals of Indian Academy of Neurology

Chromosome 1p31.1 Deletion Syndrome: Limited Expression.

Seba Biswal et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

3 papers cite it

2022
2023
2024
2025
cites it
Full record →Abstract, authors, funding and every citing paper · PMID 33911383