Associated Papers
A novel stop-gain pathogenic variant in FLT4 and a nonsynonymous pathogenic variant in PTPN11 associated with congenital heart defects.
Tabib A et al.
European Journal of Medical Research, 2022
A novel mutation in the conserved sequence of vascular endothelial growth factor receptor 3 leads to primary lymphoedema.
Dai T et al.
The Journal of International Medical Research, 2018
Analysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas.
Connell FC et al.
Human Genetics, 2009
Identification of a novel VEGFR-3 missense mutation in a Chinese family with hereditary lymphedema type I.
Yu Z et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao, 2007
Milroy's primary congenital lymphedema in a male infant and review of the literature.
Kitsiou-Tzeli S et al.
In Vivo (athens, Greece), 0
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