Author/Creator: Zatz, M - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Zatz, M

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
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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
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3. Autosomal dominant (AD) pure spastic paraplegia (HSP) linked to locus SPG4 affects almost exclusively males in a large pedigree. Issue 12 (1st December 2002)

Authors:: Starling, A; Rocco, P; Passos-Bueno, M R; Hazan, J; Marie, S K; Zatz, M
Journal:: Journal of medical genetics
Issue:: Volume 39:Issue 12(2002)
Page Start:: e77
Record Type:: Journal Article
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4. 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
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5. 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
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6. Different origins of mutations at the Machado-Joseph locus (MJD1). Issue 5 (May 1996)

Authors:: Iughetti, P; Zatz, M; Bueno, M R; Marie, S K
Journal:: Journal of medical genetics
Issue:: Volume 33:Issue 5(1996)
Page Start:: 439
Record Type:: Journal Article
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7. Estimate of germinal mosaicism in Duchenne muscular dystrophy. Issue 11 (November 1990)

Authors:: Passos-Bueno, M R; Lima, M A; Zatz, M
Journal:: Journal of medical genetics
Issue:: Volume 27:Issue 11(1990)
Page Start:: 727
Record Type:: Journal Article
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8. Facioscapulohumeral muscular dystrophy: aspects of genetic counselling, acceptance of preclinical diagnosis, and fitness. Issue 7 (July 1993)

Authors:: Eggers, S; Passos-Bueno, M R; Zatz, M
Journal:: Journal of medical genetics
Issue:: Volume 30:Issue 7(1993)
Page Start:: 589
Record Type:: Journal Article
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9. 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
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10. Homozygosity for autosomal dominant facioscapulohumeral muscular dystrophy (FSHD) does not result in a more severe phenotype. Issue 2 (2nd February 2004)

Authors:: Tonini, M M O; Pavanello, R C M; Gurgel-Giannetti, J; Lemmers, R J; van der Maarel, S M; Frants, R R; Zatz, M
Journal:: Journal of medical genetics
Issue:: Volume 41:Issue 2(2004)
Page Start:: e17
Record Type:: Journal Article
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