Citations for
1CDMM, FGF3, OTDD
A FGF3 mutation associated with differential inner ear malformation, microtia, and microdontia.
Ramsebner R, Ludwig M, Parzefall T, Lucas T, Baumgartner WD, Bodamer O, Cengiz FB, Schoefer C, Tekin M, Frei K.
Laryngoscope 120(2):359-64. 2010
2FGF3, OTDD
Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3).
Alsmadi O, Meyer BF, Alkuraya F, Wakil S, Alkayal F, Al-Saud H, Ramzan K, Al-Sayed M.
Eur J Hum Genet 17(1):14-21. Epub 2008 Aug 13. 2009
3FGF3, OTDD
Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia.
Tekin M, OztŸrkmen Akay H, Fitoz S, Birnbaum S, Cengiz FB, SennaroĀlu L, Incesulu A, YŸksel Konuk EB, HasanefendioĀlu Bayrak A, SentŸrk S, Cebeci I, Utine GE, Tunbilek E, Nance WE, Duman D.
Clin Genet 73(6):554-65. Epub 2008 Apr 22. 2008
4OTDD
Otodental dysplasia: a five year study.
Cook RA, Cox JR, Jorgenson RJ.
Ear Hear 2(2):90-4. 1981