P667: NEGR1 intragenic exonic deletions strengthen the association with neurodevelopmental disorders

P667: NEGR1 intragenic exonic deletions strengthen the association with neurodevelopmental disorders

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Bibliographic Details
Main Authors:	Yunjia Chen, Min Gao, Caterina Abdala Villa, Andrew Carroll, Fady Mikhail
Format:	Article
Language:	English
Published:	Elsevier 2025-01-01
Series:	Genetics in Medicine Open
Online Access:	http://www.sciencedirect.com/science/article/pii/S2949774425010751
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