The genetics of auricular development and malformation: New findings in model systems driving future directions for microtia research

Author:

Cox Timothy C.ORCID,Camci Esra D.,Vora Siddharth,Luquetti Daniela V.ORCID,Turner Eric E.

Funder

Laurel Foundation Endowment for Craniofacial Research

American Association of Orthodontics Foundation

University of Washington, School of Dentistry Institutional Trainee Award

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference71 articles.

1. Eya1-Six1 interaction is sufficient to induce hair cell fate in the cochlea by activating Atoh1 expression in cooperation with Sox2;Ahmed;Dev. Cell,2012

2. Genetics of microtia and associated syndromes;Alasti;J. Med. Genet.,2009

3. A mutation in HOXA2 is responsible for autosomal-recessive microtia in an Iranian family;Alasti;Am. J. Med. Genet.,2008

4. Hox genes and segmentation of the hindbrain and axial skeleton;Alexander;Annu. Rev. Cell Dev. Biol.,2009

5. The association of facial palsy and/or sensorineural hearing loss in patients with hemifacial microsomia;Bassila;Cleft Palate J.,1989

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