Spectrum of Mutations in USH2A in British Patients with Usher Syndrome Type II

By Leroy B.P.   Aragon-Martin J.A.   Weston M.D.   Bessant D.A.R.   Willis C.   Webster A.R.   Bird A.C.   Kimberling W.J.   Payne A.M.   Bhattacharya S.S.  

Experimental Eye Research, Vol. 72, Iss. 5, 2001-05 ,pp. : 503-509

Elsevier

Access to resources Recommend Favorite

Evaluation of the Myosin VIIA Gene and Visual Function in Patients with Usher Syndrome Type I

By Bharadwaj A.K.   Kasztejna J.P.   Huq S.   Berson E.L.   Dryja T.P.  

Experimental Eye Research, Vol. 71, Iss. 2, 2000-08 ,pp. : 173-181

Elsevier

Access to resources Recommend Favorite

The prevalence of Usher Syndrome in Sweden: a nationwide epidemiological and clinical survey

By Sadeghi Mehdi   Kimberling William   Tranebjœrg Lisbeth   Möller Claes  

Audiological Medicine, Vol. 2, Iss. 4, 2004-12 ,pp. : 220-228

Informa Healthcare

Access to resources Recommend Favorite

A rare brain developmental anomaly in a patient with Usher’s syndrome

By Demir Helin   Deniz Fatih   Yardım Hüseyin  

International Ophthalmology, Vol. 30, Iss. 1, 2010-02 ,pp. : 85-88

Springer Publishing Company

Access to resources Recommend Favorite

Genetic analysis of PAX3 for diagnosis of Waardenburg syndrome type I

By Matsunaga Tatsuo   Mutai Hideki   Namba Kazunori   Morita Noriko   Masuda Sawako  

Acta Oto-Laryngologica, Vol. 133, Iss. 4, 2013-04 ,pp. : 345-351

Informa Healthcare

Access to resources Recommend Favorite