The expanding clinical phenotype of germline ABL1‐associated congenital heart defects and skeletal malformations syndrome

Chen, Chun‐An ; Crutcher, Emeline ; Gill, Harinder ; Nelson, Tanya N. ; Robak, Laurie A. ; Jongmans, Marjolijn C. J. ; Pfundt, Rolph ; Prasad, Chitra ; Berard, Roberta A. ; Fannemel, Madeleine ; Frengen, Eirik ; Misceo, Doriana ; Ramsey, Keri ; Yang, Yaping ; Schaaf, Christian P. ; Wang, Xia

Human mutation, 2020-10, Vol.41 (10), p.1738-1744 [Periódico revisado por pares]

United States: Hindawi Limited

Texto completo disponível