PAX3 - Wikipedia
PAX3 (paired box gene 3 (Waardenburg syndrome 1))
Addgene: pISH-Pax3
A novel mutation of the PAX3 gene in a Chinese family with Waardenburg syndrome type I - Ma - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Waardenburg Syndrome, Type 3 | Hereditary Ocular Diseases
PAX3 - Wikipedia
PAX3 Protein Overview: Sequence, Structure, Function and Protein Interaction | Sino Biological
Four mutations in MITF, SOX10 and PAX3 genes were identified as genetic causes of waardenburg syndrome in four unrelated Iranian patients: case report | BMC Pediatrics | Full Text
How researchers discovered the genetic origin of the 'unibrow' and other hair traits
Fusion of the Paired Box 3 (PAX3) and Myocardin (MYOCD) Genes in Pediatric Rhabdomyosarcoma | Cancer Genomics & Proteomics
PAX3 Gene - GeneCards | PAX3 Protein | PAX3 Antibody
Identification and functional analysis of a novel mutation in the PAX3 gene associated with Waardenburg syndrome type I - ScienceDirect
Myo-differentiation reporter screen reveals NF-Y as an activator of PAX3–FOXO1 in rhabdomyosarcoma | PNAS
Double heterozygous mutations of MITF and PAX3 result in Waardenburg syndrome with increased penetrance in pigmentary defects - Yang - 2013 - Clinical Genetics - Wiley Online Library
PAX3-NCOA2 fusion gene has a dual role in promoting the proliferation and inhibiting the myogenic differentiation of rhabdomyosarcoma cells | Oncogene
Pax3/7 duplicated and diverged independently in amphioxus, the basal chordate lineage | Scientific Reports
Schematic representation of normal and aberrant splicing of the Pax-3... | Download Scientific Diagram
Transcriptome analyses based on genetic screens for Pax3 myogenic targets in the mouse embryo | BMC Genomics | Full Text
PAX3 (paired box 3) | Gene Report | BioGPS
Frontiers | Case Report: A Novel Gross Deletion in PAX3 (10.26 kb) Identified in a Chinese Family With Waardenburg Syndrome by Third-Generation Sequencing
