NR2F1 deletion in a patient with a de novo paracentric inversion, inv(5)(q15q33.2), and syndromic deafness

Published 2009 View Full Article

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Title
NR2F1 deletion in a patient with a de novo paracentric inversion, inv(5)(q15q33.2), and syndromic deafness
Authors
Keywords
-
Journal
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
Volume 149A, Issue 5, Pages 931-938
Publisher
Wiley
Online
2009-04-08
DOI
10.1002/ajmg.a.32764

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