Original Research
Published on 18 Feb 2020
Modeling Bainbridge-Ropers Syndrome in Xenopus laevis Embryos
in Developmental Physiology
Frontiers in Physiology
doi 10.3389/fphys.2020.00075
- 7,621 views
- 20 citations
8 articles related to "Asxl3"
Articles
Case Report
Published on 11 Dec 2025
Case Report: Synergistic effects of an ASXL3 mutation and a 15q11.2 BP1-BP2 microdeletion in a severe neurodevelopmental phenotype
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1674158
- 1,249 views
Original Research
Published on 14 Nov 2024
Four heterozygous de novo variants in ASXL3 identified with Bainbridge–Ropers syndrome and further dissecting published genotype–phenotype spectrum
in Neurodevelopment
Frontiers in Neuroscience
doi 10.3389/fnins.2024.1456433
- 3,031 views
- 4 citations
Original Research
Published on 06 Nov 2023
Examining the neurodevelopmental and motor phenotypes of Bohring-Opitz syndrome (ASXL1) and Bainbridge-Ropers syndrome (ASXL3)
in Neurodevelopment
Frontiers in Neuroscience
doi 10.3389/fnins.2023.1244176
- 4,810 views
- 4 citations
Original Research
Published on 22 Jan 2026
ASXL3 gene variants causing Bainbridge-Ropers syndrome: clinical and genetic analysis of four Chinese patients
in Neurodevelopment
Frontiers in Neuroscience
doi 10.3389/fnins.2025.1739877
- 831 views
Original Research
Published on 04 Sep 2025
Paternal mosaicism in ASXL3-related bainbridge-ropers syndrome: implications for genetic counseling and prenatal diagnosis
in Genetics of Common and Rare Diseases
Frontiers in Pediatrics
doi 10.3389/fped.2025.1655021
- 1,597 views
Correction
Published on 09 Jan 2026
Correction: Case Report: Synergistic effects of an ASXL3 mutation and a 15q11.2 BP1-BP2 microdeletion in a severe neurodevelopmental phenotype
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1769021
- 753 views
Original Research
Published on 28 Feb 2023
Targeted sequencing and clinical strategies in children with autism spectrum disorder: A cohort study
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2023.1083779
- 6,540 views
- 7 citations