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
2.
A 20-year Clinical and Genetic Neuromuscular Cohort Analysis in Lebanon: An International Effort.
J Neuromuscul Dis
; 9(1): 193-210, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-34602496