Abstract:
:We performed whole exome sequencing in a family with FOXC2 mutation where the phenotype in one generation was strikingly more severe. Although there were 3 mutations shared by 2 fatal fetal hydrops cases and not the mildly affected mother, none of them were likely to be the cause of the marked phenotypic change.
journal_name
Lymphologyjournal_title
Lymphologyauthors
Lai LW,Erickson RP,Bernas M,Witte MHsubject
Has Abstractpub_date
2018-01-01 00:00:00pages
85-88issue
2eissn
0024-7766issn
2522-7963journal_volume
51pub_type
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