Whole‐exome sequencing reveals novel USP9X variant in female fetus with isolated agenesis of the corpus callosum von Lenberg, Jerica L., Pretorius, Dolores H., Rupe, Eric S., Jones, Marilyn C., Ramos, Gladys A., Andreasen, Tara S.

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Maternal and fetal capillary malformation-arteriovenous malformation (CM-AVM) due to a novel RASA1 mutation presenting with prenatal non-immune hydrops fetalis von Overcash, Rachael T., Gibu, Christopher K., Jones, Marilyn C., Ramos, Gladys A., Andreasen, Tara S.

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Novel mutation in CCBE 1 as a cause of recurrent hydrops fetalis from Hennekam lymphangiectasia‐lymphedema syndrome‐1 von 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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Whole-exome sequencing reveals novel USP9X variant in female fetus with isolated agenesis of the corpus callosum von Lenberg, Jerica L, Pretorius, Dolores H, Rupe, Eric S, Jones, Marilyn C, Ramos, Gladys A, Andreasen, Tara S

Volltext

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