DOI:
10.1055/s-00000015
European Journal of Pediatric Surgery
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References
Vasudevan PC, Twigg SR, Mulliken JB, Cook JA, Quarrell OW, Wilkie AO.
Expanding the phenotype of craniofrontonasal syndrome: two unrelated boys with EFNB1 mutations and congenital diaphragmatic hernia.
Eur J Hum Genet 2006;
14 (07) 884-887
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