Pathogenic paternally inherited NLGN4X deletion in a female with autism spectrum disorder: Clinical, cytogenetic, and molecular characterization-Reference-Cited by-同舟云学术

Pathogenic paternally inherited NLGN4X deletion in a female with autism spectrum disorder: Clinical, cytogenetic, and molecular characterization

Published:2020-12-24 Issue:3 Volume:185 Page:894-900
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Kopp Nathan¹^ORCID,Amarillo Ina²,Martinez‐Agosto Julian³^ORCID,Quintero‐Rivera Fabiola¹⁴^ORCID

Affiliation:

1. Department of Pathology and Laboratory Medicine, UCLA Clinical Genomics Center University of California, Los Angeles, David Geffen School of Medicine Los Angeles California USA

2. Department of Pathology Washington University School of Medicine St. Louis Missouri USA

3. Department of Pediatrics and Human Genetics, UCLA Clinical Genomics Center University of California, Los Angeles Los Angeles California USA

4. Department of Pathology and Laboratory Medicine University of California, Irvine Irvine California USA

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.62025

Reference32 articles.

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2. Comprehensive Analysis of Rare Variants of 101 Autism-Linked Genes in a Hungarian Cohort of Autism Spectrum Disorder Patients

3. The emerging role of synaptic cell-adhesion pathways in the pathogenesis of autism spectrum disorders

4. X-inactivation profile reveals extensive variability in X-linked gene expression in females

5. Molecular cytogenetic analysis of a familial interstitial deletion Xp22.2-22.3 with a highly variable phenotype in female carriers

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