Associated Papers
Analysis of pathogenic variants in 605 Chinese children with non-syndromic cardiac conotruncal defects based on targeted sequencing.
Ye J et al.
Genomics, 2023
Molecular diagnosis and novel genes and phenotypes in a pediatric thoracic insufficiency cohort.
Strong A et al.
Scientific Reports, 2023
36653407 (PubMed )
Supplement: 41598_2023_27641_MOESM2_ESM.xlsx › Sheet1
MESP2 variants contribute to conotruncal heart defects by inhibiting cardiac neural crest cell proliferation.
Zhang E et al.
Journal of Molecular Medicine (berlin, Germany), 2020
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