Identification of a novel microdeletion at 9q21.13

Identification of a novel microdeletion at 9q21.13 in a family with epilepsy, intellectual disability, and speech disorders and literature review

Publication Details

Journal
China National GeneBank DataBase
Published
2025-01-01
DOI
https://doi.org/10.26036/cnp0007603
Primary Topic
Genomic variations and chromosomal abnormalities
Type
article
Field-Weighted Citation Impact
0.00
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article

Identification of a novel microdeletion at 9q21.13

China National GeneBank DataBase
Genomic variations and chromosomal abnormalities
article

Identification of a novel microdeletion at 9q21.13

article en

Abstract

Identification of a novel microdeletion at 9q21.13 in a family with epilepsy, intellectual disability, and speech disorders and literature review

China National GeneBank DataBase
Quality Education
Openalex Percentile: Top 56%
Genomic variations and chromosomal abnormalities
DOIOpen Access PDFOpenAlex
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Identification of a novel microdeletion at 9q21.13 · China National GeneBank DataBase (2025) | TGRS Research Map | TGRS