Jing Xin

Foshan, China

Last Updated: 09/26/2026

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Found 9 publications

Novel LAMA1 Mutations in a Pedigree With Poretti-Boltshauser Syndrome: Implications for Hypomyelination.

Novel LAMA1 Mutations in a Pedigree With Poretti-Boltshauser Syndrome: Implications for Hypomyelination.

Journal: Molecular genetics & genomic medicine

Published: March 14, 2026

Two Atypical Cases of Adams-Oliver Syndrome With DOCK6 Genetic Variants.

Two Atypical Cases of Adams-Oliver Syndrome With DOCK6 Genetic Variants.

Journal: American journal of medical genetics. Part A

Published: December 03, 2025

Morphological features of language regions in children with autism spectrum disorder and varying language abilities.

Morphological features of language regions in children with autism spectrum disorder and varying language abilities.

Journal: Psychiatry research

Published: October 29, 2024

Qihuang needle therapy for autism spectrum disorder with sleep disorder: a multi-center randomized controlled trial

Qihuang needle therapy for autism spectrum disorder with sleep disorder: a multi-center randomized controlled trial

Journal: Zhongguo zhen jiu = Chinese acupuncture & moxibustion

Published: September 06, 2024

Acoustic Exaggeration Enhances Speech Discrimination in Young Autistic Children.

Acoustic Exaggeration Enhances Speech Discrimination in Young Autistic Children.

Journal: Autism research : official journal of the International Society for Autism Research

Published: July 26, 2024

Atypical brain lateralization for speech processing at the sublexical level in autistic children revealed by fNIRS.

Atypical brain lateralization for speech processing at the sublexical level in autistic children revealed by fNIRS.

Journal: Scientific reports

Published: August 10, 2023

A syndrome featuring developmental disorder of the nervous system induced by a novel mutation in the TCF20 gene, rarely concurrent immune disorders: a case report.

A syndrome featuring developmental disorder of the nervous system induced by a novel mutation in the TCF20 gene, rarely concurrent immune disorders: a case report.

Journal: Frontiers in genetics

Published: March 23, 2023

Absence of associations with prefrontal cortex and cerebellum may link to early language and social deficits in preschool children with ASD.

Absence of associations with prefrontal cortex and cerebellum may link to early language and social deficits in preschool children with ASD.

Journal: Frontiers in psychiatry

Published: January 15, 2023

Genotype-phenotype implications from three representative clinical FOXG1 variants associated with FOXG1 syndrome.

Genotype-phenotype implications from three representative clinical FOXG1 variants associated with FOXG1 syndrome.

Journal: Seizure

Published: December 19, 2020

Showing 1-9 of 9

Last Updated: 09/26/2026