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Paper Details

FBN1 contributing to familial congenital diaphragmatic hernia.
Am J Med Genet A
22
2015
4970insA, CDH, CDH-related genes, Congenital diaphragmatic hernia, DES, ES, FBN1, FBN1 mutations, FREM1, MET, Marfan syndrome, PAX3, birth defect, diaphragm defects, ectopia lentis, familial CDH, familial congenital diaphragmatic hernia, fibrillin 1 gene, humans, mice, p, paraesophageal hernias

Datasets

Release 1.2