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7p22.3 microdeletion: a case study of a patient with congenital heart defect, neurodevelopmental delay and epilepsy.

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Bibliographic Details
Title:	7p22.3 microdeletion: a case study of a patient with congenital heart defect, neurodevelopmental delay and epilepsy.
Authors:	Skvortsova, Liliya¹ (AUTHOR), Perfilyeva, Anastassiya¹ (AUTHOR), Bespalova, Kira^1,2 (AUTHOR) Kira.b.bespalova@gmail.com, Kuzovleva, Yelena¹ (AUTHOR), Kabysheva, Nailya¹ (AUTHOR), Khamdiyeva, Ozada^1,2 (AUTHOR)
Source:	Orphanet Journal of Rare Diseases. 8/16/2024, Vol. 19 Issue 1, p1-9. 9p.
Database:	Academic Search Ultimate
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Description
ISSN:	17501172
DOI:	10.1186/s13023-024-03321-8