The expanding clinical phenotype of germline ABL1‐associated congenital heart defects and skeletal malformations syndrome
Human mutation, 2020-10, Vol.41 (10), p.1738-1744 [Peer Reviewed Journal]2020 Wiley Periodicals LLC ;2020 Wiley Periodicals LLC. ;info:eu-repo/semantics/openAccess ;ISSN: 1059-7794 ;EISSN: 1098-1004 ;DOI: 10.1002/humu.24075 ;PMID: 32643838
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