Detalhe da pesquisa
1.
Homozygous deletion of exons 2-7 within TGFB3 gene in a child with severe Loeys-Dietz syndrome and Marfan-like features.
Am J Med Genet A
; 182(5): 1230-1235, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32022420