DOI:
10.1055/s-00000015
European Journal of Pediatric Surgery
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References
Hogue J, Shankar S, Perry H, Patel R, Vargervik K, Slavotinek A.
A novel EFNB1 mutation (c.712delG) in a family with craniofrontonasal syndrome and diaphragmatic hernia.
Am J Med Genet A 2010;
152A (10) 2574-2577
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