| 1 | CDMM, 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
|
| 2 | FGF3, 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
|
| 3 | FGF3, OTDD
|
| Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia.
|
| Tekin M, Oztrkmen Akay H, Fitoz S, Birnbaum S, Cengiz FB, Sennarolu L, Incesulu A, Yksel Konuk EB, Hasanefendiolu Bayrak A, Sentrk S, Cebeci I, Utine GE, Tunbilek E, Nance WE, Duman D.
|
| Clin Genet 73(6):554-65. Epub 2008 Apr 22. 2008
|
| 4 | OTDD
|
| Otodental dysplasia: a five year study.
|
| Cook RA, Cox JR, Jorgenson RJ.
|
| Ear Hear 2(2):90-4. 1981
|