Broadening the phenotype associated with mutations in UPF3B: Two further cases with renal dysplasia and variable developmental delay

Published 2012 View Full Article

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Title
Broadening the phenotype associated with mutations in UPF3B: Two further cases with renal dysplasia and variable developmental delay
Authors
Keywords
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Journal
European Journal of Medical Genetics
Volume 55, Issue 8-9, Pages 476-479
Publisher
Elsevier BV
Online
2012-04-26
DOI
10.1016/j.ejmg.2012.03.010

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