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 aipamenaVasudevan, 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 aipamenaVasudevan, P., et al. Expanding the Phenotype of Craniofrontonasal Syndrome: Two Unrelated Boys with EFNB1 Mutations and Congenital Diaphragmatic Hernia. 2006.
Kontuz: berrikusi erreferentzia hauek erabili aurretik.