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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.

Today in Pediatrics...keeping you current

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Adolescent type 1 Diabetes cardio-renal Intervention Trial
BMC Pediatrics, 12/18/09