1. A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies. Issue 11 (November 1998) Authors: Moreira, E S; Vainzof, M; Marie, S K; Nigro, V; Zatz, M; Passos-Bueno, M R Journal: Journal of medical genetics Issue: Volume 35:Issue 11(1998) Page Start: 951 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A novel locus for late onset amyotrophic lateral sclerosis/motor neurone disease variant at 20q13. Issue 4 (1st April 2004) Authors: Nishimura, A L; Mitne-Neto, M; Silva, H C A; Oliveira, J R M; Vainzof, M; Zatz, M Journal: Journal of medical genetics Issue: Volume 41:Issue 4(2004) Page Start: 315 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Cosegregation of schizophrenia with Becker muscular dystrophy: susceptibility locus for schizophrenia at Xp21 or an effect of the dystrophin gene in the brain?. Issue 2 (February 1993) Authors: Zatz, M; Vallada, H; Melo, M S; Passos-Bueno, M R; Vieira, A H; Vainzof, M; Gill, M; Gentil, V Journal: Journal of medical genetics Issue: Volume 30:Issue 2(1993) Page Start: 131 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. CTG repeat length in muscle from patients affected with myotonic dystrophy (DM). Issue 2 (February 1996) Authors: Zatz, M; Passos-Bueno, M R; Cerqueira, A; Vainzof, M Journal: Journal of medical genetics Issue: Volume 33:Issue 2(1996) Page Start: 173 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in Brazilian families. Issue 5 (May 1993) Authors: Passos-Bueno, M R; Richard, I; Vainzof, M; Fougerousse, F; Weissenbach, J; Broux, O; Cohen, D; Akiyama, J; Marie, S K; Carvalho, A A Journal: Journal of medical genetics Issue: Volume 30:Issue 5(1993) Page Start: 385 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genotype-phenotype correlations in 35 Brazilian families with sarcoglycanopathies including the description of three novel mutations. Issue 2 (1st February 2003) Authors: Moreira, E S; Vainzof, M; Suzuki, O T; Pavanello, R C M; Zatz, M; Passos-Bueno, M R Journal: Journal of medical genetics Issue: Volume 40:Issue 2(2003) Page Start: e12 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian families. Issue 2 (February 1996) Authors: Passos-Bueno, M R; Moreira, E S; Marie, S K; Bashir, R; Vasquez, L; Love, D R; Vainzof, M; Iughetti, P; Oliveira, J R; Bakker, E; Strachan, T; Bushby, K; Zatz, M Journal: Journal of medical genetics Issue: Volume 33:Issue 2(1996) Page Start: 97 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Myotonic dystrophy: genetic, clinical, and molecular analysis of patients from 41 Brazilian families. Issue 1 (January 1995) Authors: Passos-Bueno, M R; Cerqueira, A; Vainzof, M; Marie, S K; Zatz, M Journal: Journal of medical genetics Issue: Volume 32:Issue 1(1995) Page Start: 14 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Segregation distortion of the CTG repeats at the myotonic dystrophy (DM) locus: new data from Brazilian DM families. Issue 9 (September 1997) Authors: Zatz, M; Cerqueira, A; Vainzof, M; Passos-Bueno, M R Journal: Journal of medical genetics Issue: Volume 34:Issue 9(1997) Page Start: 790 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. The effect of calpain 3 deficiency on the pattern of muscle degeneration in the earliest stages of LGMD2A. Issue 8 (30th July 2003) Authors: Vainzof, M; de Paula, F; Tsanaclis, A M; Zatz, M Journal: Journal of clinical pathology Issue: Volume 56:Issue 8(2003) Page Start: 624 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗