Cited by 40

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Genetic testing impacts the utility of prospective familial screening in hypertrophic cardiomyopathy through identification of a nonfamilial subgroup

Ko, Carol, Arscott, Patricia, Concannon, Maryann, Saberi, Sara, Day, Sharlene M., Yashar, Beverly M., Helms, Adam S.·2018·Genetics in Medicine

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Crossref · 10.1038/gim.2017.79

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Research works printed but not linked: 2

  1. Walsh R, Thomson KL, Ware JS et al, Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples. Genet Med 2016;17:90. · DOI
  2. Walsh R, Buchan R, Wilk A et al, Defining the genetic architecture of hypertrophic cardiomyopathy: re-evaluating the role of non-sarcomeric genes. Eur Heart J 2017;11 (e-pub ahead of print). · DOI

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Metadata

Authors
Ko, C., Arscott, P., Concannon, M., Saberi, S., Day, S. M., Yashar, B. M., & Helms, A. S.
Venue
Genetics in Medicine
Publisher
Elsevier BV
Published
2018-01
Volume
20
Issue
1
Pages
69-75
ISSN
1098-3600
Cited by
40
References
1
Language
en

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