Whole-exome sequencing identifies USH2A mutations in a pseudo-dominant Usher syndrome family.

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Whole-exome sequencing identifies USH2A mutations in a pseudo-dominant Usher syndrome family.

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Whole-exome sequencing identif ...... ominant Usher syndrome family.

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Whole-exome sequencing identif ...... ominant Usher syndrome family.

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Whole-exome sequencing identif ...... ominant Usher syndrome family.

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Whole-exome sequencing identif ...... ominant Usher syndrome family.

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Whole-exome sequencing identif ...... ominant Usher syndrome family.

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Whole-exome sequencing identif ...... ominant Usher syndrome family.

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P1476

Whole-exome sequencing identif ...... ominant Usher syndrome family.

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P2093

Hong-Liang Zhang

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Qian-Yan Kang

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Sui-Lian Zheng

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Zhen-Lang Lin

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P2860

Whole exome sequencing identifies a mutation for a novel form of corneal intraepithelial dyskeratosis

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Molecular diagnosis of Usher syndrome: application of two different next generation sequencing-based procedures.

Targeted exome sequencing identified novel USH2A mutations in Usher syndrome families.

Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis.

Comprehensive molecular diagnosis of Bardet-Biedl syndrome by high-throughput targeted exome sequencing.

Whole-exome sequencing identifies novel compound heterozygous mutations in USH2A in Spanish patients with autosomal recessive retinitis pigmentosa

SLC7A14 linked to autosomal recessive retinitis pigmentosa.

Sociological and psychological factors associated with hearing loss.

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1035-1041

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scholarly article

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10.3892/IJMM.2015.2322

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2015-08-24T00:00:00Z

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281340298

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26310143

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4564089

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