Last Updated: 09/26/2026
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Found 3 publications
Damaging variants in FOXI3 cause microtia and craniofacial microsomia.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: July 01, 2022
An ancient founder mutation located between ROBO1 and ROBO2 is responsible for increased microtia risk in Amerindigenous populations.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: May 18, 2022
HOXA2 haploinsufficiency in dominant bilateral microtia and hearing loss.
Journal: Human mutation
Published: March 29, 2013
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Last Updated: 09/26/2026