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M Zatz

Showing results (171-180 of 252) with videos related to

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Journal of the Neurological Sciences|May 1, 1991
Limb-girdle syndrome: a genetic study of 22 large Brazilian families. Comparison with X-linked Duchenne and Becker dystrophiesM R Passos-Bueno, M Vainzof, R de C Pavanello, et al.
Neuromuscular Disorders : NMD|July 16, 2002
Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye?M M O Tonini, M R Passos-Bueno, A Cerqueira, et al.
Journal of Medical Genetics|March 1, 1990
Screening of deletions in the dystrophin gene with the cDNA probes Cf23a, Cf56a, and Cf115M R Passos-Bueno, D Rapaport, D Love, et al.
Brain & Development|January 1, 1996
Congenital muscular dystrophy with cerebral white matter hypodensity. Correlation of clinical features and merosin deficiencyU C Reed, S K Marie, M Vainzof, et al.
Neuromuscular Disorders : NMD|December 1, 1996
The phenotype of chromosome 2p-linked limb-girdle muscular dystrophyI Mahjneh, M R Passos-Bueno, M Zatz, et al.
American Journal of Medical Genetics|August 15, 1994
Knobloch syndrome in a large Brazilian consanguineous family: confirmation of autosomal recessive inheritanceM R Passos-Bueno, S K Marie, M Monteiro, et al.
Human Mutation|January 1, 1997
Novel point mutations in the dystrophin geneR Sitnik, S Campiotto, M Vainzof, et al.
American Journal of Medical Genetics|December 1, 1988
Effect of mazindol on growth hormone levels in patients with Duchenne muscular dystrophyM Zatz, D Rapaport, M Vainzof, et al.
American Journal of Medical Genetics|February 1, 1988
Relation between height and clinical course in Duchenne muscular dystrophyM Zatz, D Rapaport, M Vainzof, et al.
Human Molecular Genetics|June 1, 1996
A gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3A L Sertié, M Quimby, E S Moreira, et al.
Pageof 26

Showing results (171-180 of 252) with videos related to

Sort By:
Pageof 26
Journal of the Neurological Sciences|May 1, 1991
Limb-girdle syndrome: a genetic study of 22 large Brazilian families. Comparison with X-linked Duchenne and Becker dystrophiesM R Passos-Bueno, M Vainzof, R de C Pavanello, et al.
Neuromuscular Disorders : NMD|July 16, 2002
Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye?M M O Tonini, M R Passos-Bueno, A Cerqueira, et al.
Journal of Medical Genetics|March 1, 1990
Screening of deletions in the dystrophin gene with the cDNA probes Cf23a, Cf56a, and Cf115M R Passos-Bueno, D Rapaport, D Love, et al.
Brain & Development|January 1, 1996
Congenital muscular dystrophy with cerebral white matter hypodensity. Correlation of clinical features and merosin deficiencyU C Reed, S K Marie, M Vainzof, et al.
Neuromuscular Disorders : NMD|December 1, 1996
The phenotype of chromosome 2p-linked limb-girdle muscular dystrophyI Mahjneh, M R Passos-Bueno, M Zatz, et al.
American Journal of Medical Genetics|August 15, 1994
Knobloch syndrome in a large Brazilian consanguineous family: confirmation of autosomal recessive inheritanceM R Passos-Bueno, S K Marie, M Monteiro, et al.
Human Mutation|January 1, 1997
Novel point mutations in the dystrophin geneR Sitnik, S Campiotto, M Vainzof, et al.
American Journal of Medical Genetics|December 1, 1988
Effect of mazindol on growth hormone levels in patients with Duchenne muscular dystrophyM Zatz, D Rapaport, M Vainzof, et al.
American Journal of Medical Genetics|February 1, 1988
Relation between height and clinical course in Duchenne muscular dystrophyM Zatz, D Rapaport, M Vainzof, et al.
Human Molecular Genetics|June 1, 1996
A gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3A L Sertié, M Quimby, E S Moreira, et al.
Pageof 26