Published in Laryngoscope on April 01, 1990
Autosomal dominant stapes ankylosis with broad thumbs and toes, hyperopia, and skeletal anomalies is caused by heterozygous nonsense and frameshift mutations in NOG, the gene encoding noggin. Am J Hum Genet (2002) 1.16
Mutations in the NOG gene are commonly found in congenital stapes ankylosis with symphalangism, but not in otosclerosis. Clin Genet (2012) 0.88
Identification of two novel mutations in the NOG gene associated with congenital stapes ankylosis and symphalangism. J Hum Genet (2014) 0.76
Surgery for congenital anomalies of the middle ear with mobile stapes. Eur Arch Otorhinolaryngol (1993) 0.75
A novel nonsense mutation in the NOG gene causes familial NOG-related symphalangism spectrum disorder. Hum Genome Var (2016) 0.75
The gene for X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery (DFN3) is linked to PGK. Hum Genet (1988) 1.47
Fibroinflammatory pseudotumor of the ear. A locally destructive benign lesion. Arch Otolaryngol Head Neck Surg (1995) 1.01
Classification of congenital middle ear anomalies. Report on 144 ears. Ann Otol Rhinol Laryngol (1993) 0.96
Isolated congenital stapes ankylosis: surgical results in 32 ears and a review of the literature. Laryngoscope (1990) 0.87
Persistent stapedial artery: does it prevent successful surgery? Ann Otol Rhinol Laryngol (1993) 0.86
The effect of the "floating mass transducer" in the middle ear on hearing sensitivity. Am J Otol (2000) 0.80
Noninvasive assessment of the intralabyrinthine pressure. A new technique applied to patients with X-linked progressive mixed deafness syndrome with perilymphatic gusher during stapes surgery. Arch Otolaryngol Head Neck Surg (1995) 0.75
Usher syndrome. A temporal bone report. Arch Otolaryngol Head Neck Surg (1995) 0.75
Speech recognition in patients after successful surgery for unilateral congenital ear anomalies. Laryngoscope (1994) 0.75