Otros
Congenial heart disease revealing familial Velocardiofacial syndrome caused by 3 Mb deletion at 22q11 region
Fecha
2018-10-01Registro en:
European Journal Of Human Genetics. London: Nature Publishing Group, v. 26, p. 962-962, 2018.
1018-4813
WOS:000489312608082
Autor
Universidade Federal de Goiás (UFG)
Universidade Estadual Paulista (Unesp)