Novel mutation in CCBE 1 as a...

Clinical Case Reports 2018 / 10

Novel mutation in CCBE 1 as a cause of recurrent hydrops fetalis from Hennekam lymphangiectasia-lymphedema syndrome-1

Melber, Dora J., Andreasen, Tara S., Mao, Rong, Tvrdik, Tatiana, Miller, Christine E., Moore, Thomas R., Woelkers, Douglas A., Lamale-Smith, Leah M.
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Language:
english
Journal:
Clinical Case Reports
DOI:
10.1002/ccr3.1804
Date:
October, 2018
File:
PDF, 556 KB
english, 2018
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