Associated Papers
ASXL3-related disorder: Molecular phenotyping and comprehensive review providing insights into disease mechanism.
Woods E et al.
Clinical Genetics, 2024
Novel mutation in the ASXL3 gene in a Chinese boy with microcephaly and speech impairment: A case report.
Li JR et al.
World Journal of Clinical Cases, 2020
Novel de novo frameshift variant in the ASXL3 gene in a child with microcephaly and global developmental delay.
Wayhelova M et al.
Molecular Medicine Reports, 2019
Novel compound heterozygous ASXL3 mutation causing Bainbridge-ropers like syndrome and primary IGF1 deficiency.
Giri D et al.
International Journal of Pediatric Endocrinology, 2017
De novo frameshift mutation in ASXL3 in a patient with global developmental delay, microcephaly, and craniofacial anomalies.
Dinwiddie DL et al.
Bmc Medical Genomics, 2013
24044690 (PubMed )
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