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Title
What Is New in Genetics of Congenital Heart Defects?
Authors
Keywords
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Journal
Frontiers in Pediatrics
Volume 4, Issue -, Pages -
Publisher
Frontiers Media SA
Online
2016-12-01
DOI
10.3389/fped.2016.00120
References
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Related references
Note: Only part of the references are listed.- Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation
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- Fine Mapping of the 1p36 Deletion Syndrome Identifies Mutation of PRDM16 as a Cause of Cardiomyopathy
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- Left-ventricular non-compaction (LVNC): A clinical feature more often observed in terminal deletion 1p36 than previously expected
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- NOTCH1 mutations in individuals with left ventricular outflow tract malformations reduce ligand-induced signaling
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- (2008) Heather C. Mefford et al. NEW ENGLAND JOURNAL OF MEDICINE
- Further Delineation of Deletion 1p36 Syndrome in 60 Patients: A Recognizable Phenotype and Common Cause of Developmental Delay and Mental Retardation
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