1. Waardenburg syndrome;Read;J. Med. Genet.,1997
2. Waardenburg syndrome (WS): the analysis of a single family with a WS1 mutation showing linkage to RFLP markers on human chromosome 2q;Asher;Am. J. Hum. Genet.,1991
3. Dual embryonic origin of the mammalian otic vesicle forming the inner ear;Freyer;Development,2011
4. Pax3 and hippo signaling coordinate melanocyte gene expression in neural crest;Manderfield;Cell Rep.,2014
5. PAX3 and PAX7 as upstream regulators of myogenesis;Buckingham;Semin. Cell Dev. Biol.,2015