GuildSR: A case of bilateral scala communis cochleae uncomplicated by other defects. An embryological interpretation of this and associated anomalies. Anat Rec42: 19, 1929.
7.
GussenR: Mondini type of genetically determined deafness. J Laryngol82: 41–55, 1968.
8.
KosAOSchuknechtHFSingerJ: Temporal bone studies in 13–15 and 18 trisomy syndromes. Arch Otolaryng83: 439–445, 1966.
9.
MeyersENStoolSWeltschewA: Congenital anomaly of the middle and inner ear. Laryngoscope78: 344–351, 1968.
10.
MichelEM: Memoire sur les anomalies congenitales de l'oreille interne. Gazette Medicale de Strasbourg3: 55–58, 1863.
11.
MondiniC: As cited by Altmann F. The inner ear in genetically determined deafness. Acta Oto-laryng Suppl187: 1–39, 1964.
12.
MurakamiYSchuknechtHF: Unusual congenital anomalies in the inner ear. Arch Otolaryng87: 335–349, 1968.
13.
NagerFR: Missbildungen der Schnecke und hörvermögen. Ztschr f Hals-Nasen-u Ohrenheilk11: 149–176, 1925.
14.
OrmerodFC: Pathology of congenital deafness. J Laryngol74: 919–950, 1960.
15.
PolvogtLMCroweSJ: Anomalies of the cochlea in patients with normal hearing. Ann Otol46: 579–591, 1937.
16.
ScheibeA: Ein fall von taubstummheit mit akusticusatriphie und bildungsanomalien im hautigen labyrinth beiderseits. Ztschr f Ohrenheilk22: 11–23, 1891–92.
17.
SecrétanJP: De l'histologie normale du sac endolymphatique chez l'homme. Acta Otolaryng32: 119–163, 1944.
