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8p21.3 deletions are rare causes of non-syndromic autism spectrum disorder

Document Type

Article

Author

Cosemans, N.; Vogels, A.; Holvoet, M.; Devriendt, K.; Van Den Bogaert, K.; Peeters, H.; Maljaars, J.; Steyaert, J.; Noens, I.

Source

In: Neurogenetics. (Neurogenetics, July 2021, 22(3):207-213)

Subject

Language

English

ISSN

13646753
13646745

Online Access

Full Text (ProQuest Central) Web of Science JCR 저널정보 Scopus Find it@PNU

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