Vasudevan, P., Twigg, S., Mulliken, J., Cook, J., Quarrell, O., & Wilkie, A. (2006). Expanding the phenotype of craniofrontonasal syndrome: Two unrelated boys with EFNB1 mutations and congenital diaphragmatic hernia.
Chicago Style (17th ed.) CitationVasudevan, P., SR Twigg, J. Mulliken, J. Cook, O. Quarrell, and A. Wilkie. Expanding the Phenotype of Craniofrontonasal Syndrome: Two Unrelated Boys with EFNB1 Mutations and Congenital Diaphragmatic Hernia. 2006.
MLA citiranjeVasudevan, P., et al. Expanding the Phenotype of Craniofrontonasal Syndrome: Two Unrelated Boys with EFNB1 Mutations and Congenital Diaphragmatic Hernia. 2006.
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