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Genetic and Phenotype Analysis of a Chinese Cohort of Infants and Children With Epilepsy.
Front Genet. 2022 Apr 27;13:869210. doi: 10.3389/fgene.2022.869210. eCollection 2022.
Front Genet. 2022.
PMID: 35571021
Free PMC article.
Exons deletion of CNKSR2 gene identified in X-linked syndromic intellectual disability.
Daoqi M, Guohong C, Yuan W, Zhixiao Y, Kaili X, Shiyue M.
Daoqi M, et al. Among authors: shiyue m.
BMC Med Genet. 2020 Apr 3;21(1):69. doi: 10.1186/s12881-020-01004-2.
BMC Med Genet. 2020.
PMID: 32245427
Free PMC article.
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