Phenotypes in Defined Genotypes Including Siblings with Usher Syndrome

By Malm Eva   Ponjavic Vesna   Mööller Claes   Kimberling William J.   Andrééasson Sten  

Ophthalmic Genetics, Vol. 32, Iss. 2, 2011-06 ,pp. : 65-74

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Audiological findings in Usher syndrome types IIa and II (non-IIa)

By Sadeghi Mehdi   Cohn Edward   Kelly William   Kimberling William   Tranebjoerg Lisbeth   Möller Claes  

International Journal of Audiology, Vol. 43, Iss. 3, 2004-03 ,pp. : 136-143

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Expressivity of hearing loss in cases with Usher syndrome type IIA

By Sadeghi André M.   Cohn Edward S.   Kimberling William J.   Halvarsson Glenn   Möller Claes  

International Journal of Audiology, Vol. 52, Iss. 12, 2013-12 ,pp. : 832-837

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Novel Mutations in MYO7A and USH2A in Usher Syndrome

By Maubaret Cécilia   Griffoin Jean-Michel   Arnaud Bernard   Hamel Christian  

Ophthalmic Genetics, Vol. 26, Iss. 1, 2005-03 ,pp. : 25-29

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A novel 5-bp deletion in Clarin 1 in a family with Usher syndrome

By Akoury Elie   El Zir Elie   Mansour Ahmad   Mégarbané André   Majewski Jacek   Slim Rima  

Ophthalmic Genetics, Vol. 32, Iss. 4, 2011-11 ,pp. : 245-249

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