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By Litt Michael  

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Oxford University Press

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Exome Sequencing Identifies a Dominant TNNT3 Mutation in a Large Family with Distal Arthrogryposis

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A 5-base insertion in the γC-crystallin gene is associated with autosomal dominant variable zonular pulverulent cataract

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Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13

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Human Molecular Genetics, Vol. 20, Iss. 7, 2011-04 ,pp. : 1285-1289

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A deletion mutation in the βA1/A3 crystallin gene (CRYBA1/A3) is associated with autosomal dominant congenital nuclear cataract in a Chinese family

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