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
FLT4 Mutations Are Associated with Segmental Lymphatic Dysfunction and Initial Lymphatic Aplasia in Patients with Milroy Disease.
Liu N et al.
Genes, 2021
Identification of rare variants in novel candidate genes in pulmonary atresia patients by next generation sequencing.
Shi X et al.
Computational and Structural Biotechnology Journal, 2020
32128068 (PubMed )
Supplement: mmc2.xlsx › Table_S3
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