Not the End of the Odyssey: Parental Perceptions of Whole Exome Sequencing (WES) in Pediatric Undiagnosed Disorders-Reference-Cited by-同舟云学术

Not the End of the Odyssey: Parental Perceptions of Whole Exome Sequencing (WES) in Pediatric Undiagnosed Disorders

Published:2016-02-12 Issue:5 Volume:25 Page:1019-1031
ISSN:1059-7700
Container-title:Journal of Genetic Counseling
language:en
Short-container-title:J Genet Counsel

Author:

Rosell Allyn McConkie,Pena Loren D. M.,Schoch Kelly,Spillmann Rebecca,Sullivan Jennifer,Hooper Stephen R.,Jiang Yong-Hui,Mathey-Andrews Nicolas,Goldstein David B.,Shashi Vandana

Funder

Duke University

Publisher

Wiley

Subject

Genetics (clinical)

Link

http://link.springer.com/content/pdf/10.1007/s10897-016-9933-1.pdf

Reference37 articles.

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3. Ashtiani, S., Makela, N., Carrion, P., & Austin, J. (2014). Parents' experiences of receiving their child's genetic diagnosis: a qualitative study to inform clinical genetics practice. Am J Med Genet A, 164a(6), 1496–1502. doi: 10.1002/ajmg.a.36525 .

4. Bergner, A. L., Bollinger, J., Raraigh, K. S., Tichnell, C., Murray, B., Blout, C. L., et al. (2014). Informed consent for exome sequencing research in families with genetic disease: the emerging issue of incidental findings. Am J Med Genet A, 164a(11), 2745–2752. doi: 10.1002/ajmg.a.36706 .

5. Campbell, J. L., Quincy, C., Osserman, J., & Pedersen, O. K. (2013). Coding In-Depth Semistructured Interviews: Problems of Unitization and Intercoder Reliability and Agreement. Sociological Methods & Research, 42(3), 294–320. doi: 10.1177/0049124113500475 .

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