Amanda E. Smith

Amanda E. Smith

Pediatrics | Internal Medicine

211 Fountain Court
Suite 120
Lexington, KY 40509

Last Updated: 09/26/2026

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Found 1 publications

Chromosome 16p13.11 Microdeletion Syndrome in a Newborn: A Case Study.

Chromosome 16p13.11 Microdeletion Syndrome in a Newborn: A Case Study.

Journal: Neonatal network : NN

Published: December 21, 2018

Showing 1-1 of 1

Last Updated: 09/26/2026