Usher syndrome type I associated with bronchiectasis and immotile nasal cilia in two brothers.

Author:

Bonneau D,Raymond F,Kremer C,Klossek J M,Kaplan J,Patte F

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference11 articles.

1. Usher's syndrome: ophthalmic and neuro-otologic findings suggesting genetic heterogeneity;Fishman, G.A.; Kumar, A.; Joseph, M.E.; Torok, N.; Anderson, R.J.;Arch Ophthalmol,1983

2. Usher syndrome: definition and estimate of prevalence from two high-risk populations;Boughman, J.A.; Vernon, M.; Shaver, K.A.;J Chron Dis,1983

3. Comparison of three methods for measuring nasal mucociliary clearance in man;Puchelle, E.; Aug, F.; Bertrand, A.;Acta Otolaryngol

4. Abnormal sperm and photoreceptor axonemes in Usher's syndrome;Hunter, D.G.; Fishman, G.A.; Mehta, R.S.; Kretzer, F.L.;Arch Ophthalmol,1986

5. Histopathology of the inner ear in Usher's syndrome as observed by light and electron microscopy;Shinkawa, H.; Nadol, J.B.;Ann Otol Rhinol Laryngol,1986

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