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ArticleOrphanet journal of rare diseases2024

Genetic insights into the 'sandwich fusion' subtype of Klippel-Feil syndrome: novel FGFR2 mutations identified by 21 cases of whole-exome sequencing.

Nanfang Xu et al.PubMed ↗Full text ↗Publisher ↗

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2 papers cite it

2024
2025
2026
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Full record →Abstract, authors, funding and every citing paper · PMID 38561822