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Article

A novel homozygous deletion in CCDC32 gene causing cardiofacioneurodevelopmental syndrome: the fourth patient reported.

Clinical dysmorphology - 1 Jul 2024

Fernandes da Rocha Diogo, Quental Rita, Grangeia Ana, Pinto Moura Carla

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 38818818
DOI: 10.1097/MCD.0000000000000501

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