P272: Uniparental disomy of chromosome 19 in an individual with oculocutaneous albinism, neurodevelopmental disorder, and failure to thrive

Bibliographic Details
Main Authors:	Rebecca Procopio, Adele Schneider
Format:	Article
Language:	English
Published:	Elsevier 2023-01-01
Series:	Genetics in Medicine Open
Online Access:	http://www.sciencedirect.com/science/article/pii/S294977442300300X

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