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See Latest ArticlesSporadic In Utero Generalized Edema Caused by Mutations in the Lymphangiogenic Genes VEGFR3 and FOXC2
The Journal of Pediatrics, 07/01/09
Ghalamkarpour A et al. - Mutations in the VEGFR3 and FOXC2 genes account for a subset of patients with unexplained in utero generalized subcutaneous edema and hydrops fetalis without family history of lymphedema. Lymphangiogenic genes should be screened for mutations in sporadic patients diagnosed with fetal edema.
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Morphometric analysis and classification of the facial phenotype associated with fetal alcohol syndrome in 5- and 12-year-old children
American Journal of Medical Genetics, 12/15/09
Severe cleidocranial dysplasia and hypophosphatasia in a child with microdeletion of the C-terminal region of RUNX2
American Journal of Medical Genetics, 12/15/09
Gene expression using microarrays in transplant recipients at risk of EBV lymphoproliferation after organ transplantation
Pediatric Transplantation, 12/15/09
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