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
Molecular characterization of two novel VEGFR3 mutations in Japanese families with Milroy's disease.
Futatani T et al.
Pediatrics International : Official Journal of the Japan Pediatric Society, 2008
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