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Mutational hot spot potential of a novel base pair mutation of the CSPG2 gene in a family with Wagner syndrome. [Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't]
Arch Ophthalmol 2009 Nov; 127(11):1511-9.
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Normal spermatogenesis in a man with mutant luteinizing hormone. [Journal Article, Research Support, Non-U.S. Gov't]
N Engl J Med 2009 Nov 5; 361(19):1856-63.
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Focus on next-generation sequencing data analysis. Forward. [Introductory Journal Article]
Nat Methods 2009 Nov; 6(11 Suppl):S1.
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More on Schnyder corneal dystrophy. [Comment, Letter]
Ophthalmology 2009 Nov; 116(11):2260; author reply 2260.
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Sense from sequence reads: methods for alignment and assembly. [Journal Article, Research Support, Non-U.S. Gov't]
Nat Methods 2009 Nov; 6(11 Suppl):S6-S12.
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Computation for ChIP-seq and RNA-seq studies. [Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't]
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Next-generation gap. [Journal Article]
Nat Methods 2009 Nov; 6(11 Suppl):S2-5.
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Computational methods for discovering structural variation with next-generation sequencing. [Journal Article]
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Familial hemiplegic migraine is associated with febrile seizures in an FHM2 family with a novel de novo ATP1A2 mutation. [Case Reports, Comparative Study, Letter, Research Support, Non-U.S. Gov't]
Epilepsia 2009 Nov; 50(11):2503-4.
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Localization of Rad50, a single-copy gene, on group 5 chromosomes of wheat, using a FISH protocol employing tyramide for signal amplification (Tyr-FISH). [Journal Article, Research Support, Non-U.S. Gov't]
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