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8p23.1 microdeletion syndrome
8p23.1 deletion involves a partial deletion of the short arm of chromosome 8 characterized by low birth weight, postnatal growth deficiency, mild intellectual deficit, hyperactivity, craniofacial abnormalities, and congenital heart defects.
Tapered finger
The gradual reduction in girth of the finger from proximal to distal.
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PMID (PMCID)