A novel stop mutation in the vascular endothelial growth factor-C gene (VEGFC) results in Milroy-like disease

Mutation in Vascular Endothelial Growth Factor-C, a Ligand for Vascular Endothelial Growth Factor Receptor-3, Is Associated With Autosomal Dominant Milroy-Like Primary Lymphedema

(2013) Kristiana Gordon et al.   CIRCULATION RESEARCH

The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings

(2013) FC Connell et al.   CLINICAL GENETICS

FLT4/VEGFR3and Milroy Disease: Novel Mutations, a Review of Published Variants and Database Update

(2012) Kristiana Gordon et al.   HUMAN MUTATION

Notch restricts lymphatic vessel sprouting induced by vascular endothelial growth factor

(2011) W. Zheng et al.   BLOOD

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

(2010) A. McKenna et al.   GENOME RESEARCH

Lymphatic Dysfunction, Not Aplasia, Underlies Milroy Disease

(2010) Russell H. Mellor et al.   MICROCIRCULATION

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

(2010) K. Wang et al.   NUCLEIC ACIDS RESEARCH

Analysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas

(2008) F. C. Connell et al.   HUMAN GENETICS