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FOXC2
LE WE PMID CA
FOXC29038FOXC2

ACVRLK1

AGGF1 VG5Q

Angiogenesis

Blood vessels (Malformation)

COL3A1

ENG

Esophagus (Atresia)

FOXC2

FOXF1

Foxl1

Glomulin

Hedgehog

Klippel Trenaunay syndrome

KRIT1

MADH4

MGC4607

MTHFSD

NDP

NEMO

NOTCH3

PDCD10

PTEN MMAC1 TEP1

RASA1

SOX18

Tie2

TIMP3

VACTERL association

VEGFR3

2005  
1
Biomedicine and diseases: the Klippel-Trenaunay syndrome, vascular anomalies and vascular morphogenesis.
[15905966] Cell Mol Life Sci 62(13): 1434-47 (2005)
2008  
2
Foxc2 transcription factor: a newly described regulator of angiogenesis.
[19185813] Trends Cardiovasc Med 18(6): 224-8 (2008)
2010  
3
Genetic factors in esophageal atresia, tracheo-esophageal fistula and the VACTERL association: roles for FOXF1 and the 16q24.1 FOX transcription factor gene cluster, and review of the literature.
[19822228] Eur J Med Genet 53(1): 6-13 (2010)

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All Medline data shown were primarily retrieved from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.


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