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.
Cita Chicago (17th ed.)Vasudevan, P., SR Twigg, J. Mulliken, J. Cook, O. Quarrell, i A. Wilkie. Expanding the Phenotype of Craniofrontonasal Syndrome: Two Unrelated Boys with EFNB1 Mutations and Congenital Diaphragmatic Hernia. 2006.
Cita MLA (9th ed.)Vasudevan, P., et al. Expanding the Phenotype of Craniofrontonasal Syndrome: Two Unrelated Boys with EFNB1 Mutations and Congenital Diaphragmatic Hernia. 2006.
Atenció: Aquestes cites poden no estar 100% correctes.