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Summary Literature (5)
Literature for DOID 0060379: acrofacial dysostosis


Xenbase Articles :
( Denotes literature images)
Sf3b4-depleted Xenopus embryos: A model to study the pathogenesis of craniofacial defects in Nager syndrome., Devotta A,Juraver-Geslin H,Gonzalez JA,Hong CS,Saint-Jeannet JP, Dev Biol. July 15, 2016; 415(2):1095-564X.
Modeling human craniofacial disorders in Xenopus., Dubey A,Saint-Jeannet JP, Curr Pathobiol Rep. March 1, 2017; 5(1):2167-485X.
Mouth development., Chen J,Jacox LA,Saldanha F,Sive H, Wiley Interdiscip Rev Dev Biol. January 1, 2017; 6(5):1759-7692.
Molecular mechanisms of hearing loss in Nager syndrome., Maharana SK,Saint-Jeannet JP, Dev Biol. January 1, 2021; 476:1095-564X.
Function of chromatin modifier Hmgn1 during neural crest and craniofacial development., Ihewulezi C,Saint-Jeannet JP, Genesis. September 3, 2021; :1526-968X.