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ArticleGenes2023

A Rare Case of Concurrent 2q34q36 Duplication and 2q37 Deletion in a Neonate with Syndromic Features.

Francesco Nicola Riviello et al.PubMed ↗Full text ↗Publisher ↗

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1 paper cites it

2023
2024
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Full record →Abstract, authors, funding and every citing paper · PMID 38137016