Exome sequencing of fetuses with congenital diaphragmatic hernia supports a causal role for NR2F2, P...
Exome sequencing of fetuses with congenital diaphragmatic hernia supports a causal role for NR2F2, PTPN11, and WT1 variants
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Publisher
United States: Elsevier Inc
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Language
English
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Publisher
United States: Elsevier Inc
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Scope and Contents
Contents
To identify genes associated with congenital diaphragmatic hernia (CDH) to help understand the etiology and inform prognosis.
We performed exome sequencing on fetuses with CDH and their parents to identify rare genetic variants likely to mediate risk. We reviewed prenatal characteristics and neonatal outcomes.
Data were generated for 22 paren...
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Full title
Exome sequencing of fetuses with congenital diaphragmatic hernia supports a causal role for NR2F2, PTPN11, and WT1 variants
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TN_cdi_proquest_miscellaneous_2555966126
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2555966126
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ISSN
0002-9610
E-ISSN
1879-1883
DOI
10.1016/j.amjsurg.2021.07.016
