Using next-generation sequencing for the diagnosis of rare disorders: a family with retinitis pigmentosa and skeletal abnormalities-Reference-Cited by-同舟云学术

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

Published:2011-07-25 Issue:1 Volume:225 Page:12-18
ISSN:0022-3417
Container-title:The Journal of Pathology
language:en
Short-container-title:J. Pathol.

Author:

Schrader Kasmintan A,Heravi-Moussavi Alireza,Waters Paula J,Senz Janine,Whelan James,Ha Gavin,Eydoux Patrice,Nielsen Torsten,Gallagher Barry,Oloumi Arusha,Boyd Niki,Fernandez Bridget A,Young Terry-Lynn,Jones Steven JM,Hirst Martin,Shah Sohrab P,Marra Marco A,Green Jane,Huntsman David G

Publisher

Wiley

Subject

Pathology and Forensic Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/path.2941/fullpdf

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