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ArticleJournal of human genetics2026

Tetralogy of Fallot and craniosynostosis - differential manifestation in a familial case of CHDED syndrome caused by novel pathogenic PRKD1 variant.

Prachi Sandeep Oza et al.PubMed ↗Publisher ↗

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Full record →Abstract, authors, funding and every citing paper · PMID 41136760