Pediatrics Articles

Pediatrics

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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.

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American Journal of Medical Genetics, 12/15/09

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American Journal of Medical Genetics, 12/15/09

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