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Showing posts with label
matthew hunter
.
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Showing posts with label
matthew hunter
.
Show all posts
Monday, 6 February 2017
Interstitial deletion of chromosome 1 (1p21.1p12) in an infant with congenital diaphragmatic hernia, hydrops fetalis, and interrupted aortic arch
Arvind Sehgal, Kenneth Tan
et al
. published in
Clinical Case Reports.
Read article
here
.
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