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BioMed Central, Orphanet Journal of Rare Diseases, 1(11)

DOI: 10.1186/s13023-016-0462-7

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The rare and undiagnosed diseases diagnostic service – application of massively parallel sequencing in a state-wide clinical service

Journal article published in 2016 by Gareth Baynam, Nicholas Pachter, Fiona McKenzie, Sharon Townshend, Jennie Slee, Cathy Kiraly-Borri, Anand Vasudevan, Anne Hawkins, Stephanie Broley, Lyn Schofield, Hedwig Verhoef, Caroline E. Walker, Caron Molster, Jenefer M. Blackwell, Sarra Jamieson and other authors.
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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