AI Networking Cookbook: Practical recipes for AI-assisted network automation and development
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Expanding the KBG syndrome phenotype through 2D facial morphometry, clinical and molecular characterization
The literature review confirmed shared chromatinopathy-related features, including developmental delay, intellectual disability, craniofacial dysmorphism, skeletal anomalies and behavioral disturbances, as well as under-recognized findings such as facial asymmetry, low anterior hairline, hypotonia and hearing impairmen...