Sporadic In Utero Generalized Edema Caused by Mutations in the Lymphangiogenic Genes VEGFR3 and FOXC2-Reference-Cited by-同舟云学术

Sporadic In Utero Generalized Edema Caused by Mutations in the Lymphangiogenic Genes VEGFR3 and FOXC2

Published:2009-07 Issue:1 Volume:155 Page:90-93
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Ghalamkarpour Arash,Debauche Christian,Haan Eric,Van Regemorter Nicole,Sznajer Yves,Thomas Dominique,Revencu Nicole,Gillerot Yves,Boon Laurence M.,Vikkula Miikka

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference21 articles.

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2. Hydrops fetalis: a retrospective review of cases reported to a large national database and identification of risk factors associated with death;Abrams;Pediatrics,2007

3. Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome;Fang;Am J Hum Genet,2000

4. Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase;Irrthum;Am J Hum Genet,2000

5. Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema;Karkkainen;Nat Genet,2000

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