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ArticleBMC pediatrics2025

Long read Nanopore sequencing identifies precise breakpoints of a de novo paracentric inversion that disrupt the MEIS2 gene in a Chinese girl with syndromic developmental delay.

Jianxin Tan et al.PubMed ↗Full text ↗Publisher ↗

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2025
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Full record →Abstract, authors, funding and every citing paper · PMID 39789493