Melber, D. J., Andreasen, T. S., Mao, R., Tvrdik, T., Miller, C. E., Moore, T. R., . . . Lamale‐Smith, L. M. (2018). Novel mutation in CCBE 1 as a cause of recurrent hydrops fetalis from Hennekam lymphangiectasia‐lymphedema syndrome‐1. Clin Case Rep.
Citación estilo ChicagoMelber, Dora J., Tara S. Andreasen, Rong Mao, Tatiana Tvrdik, Christine E. Miller, Thomas R. Moore, Douglas A. Woelkers, y Leah M. Lamale‐Smith. "Novel Mutation in CCBE 1 As a Cause of Recurrent Hydrops Fetalis From Hennekam Lymphangiectasia‐lymphedema Syndrome‐1." Clin Case Rep 2018.
Cita MLAMelber, Dora J., et al. "Novel Mutation in CCBE 1 As a Cause of Recurrent Hydrops Fetalis From Hennekam Lymphangiectasia‐lymphedema Syndrome‐1." Clin Case Rep 2018.
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