J Korean Child Neurol Soc Search

CLOSE


Ann Child Neurol > Volume 23(4); 2015 > Article
Journal of the Korean Child Neurology Society 2015;23(4):165-169.
DOI: https://doi.org/10.26815/jkcns.2015.23.4.165    Published online December 30, 2015.
다양한 유형의 발작을 보인 1p36 결실증후군 1례
Key Words: Chromosome 1p36 deletion syndrome, Seizure, Microarray analysis, Comparative genomic hybridization


ABOUT
ARTICLE CATEGORY

Browse all articles >

BROWSE ARTICLES
EDITORIAL POLICY
AUTHOR INFORMATION
Editorial Office
50-1, Yonsei-ro, Seodaemun-gu, Seoul 03722, Korea
Tel: +82-2-2019-3350    Fax: +82-2-2019-4881    E-mail: editor@annchildneurol.org                

Copyright © 2019 by Korean Child Neurology Society. All rights reserved.

Developed in M2community

Close layer
prev next