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ArticleJournal of personalized medicine2023

Identification of a Novel Variant in Myelin Regulatory Growth Factor by Next-Generation Sequencing Led to the Detection of a Clinically Inapparent Congenital Heart Defect in a Patient with a 46,XY Disorder of Sex Development.

Lourdes Correa Brito 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 37511771