Expansion of the Phenotypic Spectrum of TNRC6B-Related Neurodevelopmental Disorder in a Three-Generation Family with 22q13.1 Deletion

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Publication Details

Journal
Genes
Published
2026-04-15
DOI
https://doi.org/10.3390/genes17040464
Primary Topic
Congenital heart defects research
Type
article
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article

Expansion of the Phenotypic Spectrum of TNRC6B-Related Neurodevelopmental Disorder in a Three-Generation Family with 22q13.1 Deletion

Sheridan O’Donnell, Himanshu Goel, Melissa Buckman, Nicole Bain et al.
Genes
Congenital heart defects research
article

Expansion of the Phenotypic Spectrum of TNRC6B-Related Neurodevelopmental Disorder in a Three-Generation Family with 22q13.1 Deletion

Sheridan O’Donnell, Himanshu Goel, Melissa Buckman, Nicole Bain, Jessica Archer
article en

Abstract

No abstract available for this paper.
GenesVol. 17(4)
John Hunter Hospital (AU), Hunter Genetics (AU), Tamworth Hospital (AU), University of Newcastle Australia (AU)
Quality Education
Openalex Percentile: Top 25%
Congenital heart defects research
DOIOpen Access PDFOpenAlex
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