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Publications

Title: Using next-generation sequencing for the diagnosis of rare disorders: a family with retinitis pigmentosa and skeletal abnormalities.

Authors: Schrader KA, Heravi-Moussavi A, Waters PJ, Senz J, Whelan J, Ha G, Eydoux P, Nielsen T, Gallagher B, Oloumi A, Boyd N, Fernandez BA, Young TL, Jones SJ, Hirst M, Shah SP, Marra MA, Green J, Huntsman DG.

Category: Published or in Press

Journal: J Pathol.

Volume / Issue: 255 / 1

Publication Date: 2011-09-01

Page No.: 12

PMID: 21792934

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