ArticleMolecular syndromology2022

A New Case of Rare Microdeletion 10q22.3q23 along with Mosaic Klinefelter Syndrome Associated with Facial Dysmorphic Finding, Atrial Ventricular Septal Defect, and Motor Retardation.

Firdevs Dincsoy Bir et al.PubMed ↗Full text ↗Publisher ↗

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