Reporting genomic secondary findings: ACMG members weigh in-Reference-Cited by-同舟云学术

Reporting genomic secondary findings: ACMG members weigh in

Published:2015-01 Issue:1 Volume:17 Page:27-35
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Scheuner Maren T.,Peredo Jane,Benkendorf Judith,Bowdish Bruce,Feldman Gerald,Fleisher Lynn,Mulvihill John J.,Watson Michael,Herman Gail E.,Evans James

Publisher

Elsevier BV

Subject

Genetics (clinical)

Link

http://www.nature.com/articles/gim2014165.pdf

Reference19 articles.

1. Shameer K, Klee EW, Dalenberg AK, Kullo IJ. Whole exome sequencing implicates an INO80D mutation in a syndrome of aortic hypoplasia, premature atherosclerosis, and arterial stiffness. Circ Cardiovasc Genet e-pub ahead of print 13 August 2014.

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