Browsing by Author Pavanello, RCM
Showing results 1 to 2 of 2
| Issue Date | Title | Author(s) |
| 1-Sep-2004 | Protein and DNA analysis for the prenatal diagnosis of alpha 2-laminin-deficient congenital muscular dystrophy | Yamamoto, L. U.; Gollop, T. R.; Naccache, N. F.; Pavanello, RCM; Zanoteli, E.; Zatz, M.; Vainzof, M.; Universidade de São Paulo (USP); Inst Med Fetal & Genet Humana; Universidade Federal de São Paulo (UNIFESP) |
| 15-Mar-1999 | Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian population | Vainzof, M.; Passos-Bueno, M. R.; Pavanello, RCM; Marie, S. K.; Oliveira, ASB; Zatz, M.; Universidade de São Paulo (USP); Universidade Federal de São Paulo (UNIFESP) |
