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M R Passos

Showing results (1-10 of 142) with videos related to

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American Journal of Medical Genetics|November 1, 1983
Creatine-kinase (CK) and pyruvate-kinase (PK) activities in cord blood of normal newborn infants: application to Duchenne muscular dystrophy screening programsM R Passos, M Zatz
Journal of Medical Genetics|April 1, 1991
Reproductive fitness and frequency of new mutations in Becker muscular dystrophy: implications for genetic risk estimatesM R Passos-Bueno, M Zatz
American Journal of Medical Genetics|March 1, 1989
Estimate of the proportion of Duchenne muscular dystrophy with autosomal recessive inheritanceM Zatz, M R Passos-Bueno, D Rapaport
American Journal of Medical Genetics|October 1, 1985
Creatine-kinase and pyruvate-kinase activities in normal children: implications in Duchenne muscular dystrophy carrier detectionM R Passos, C H Gonzalez, M Zatz
American Journal of Medical Genetics|October 1, 1990
Duchenne-like muscular dystrophy in the ArabsM Zatz, M R Passos-Bueno, D Rapaport
American Journal of Medical Genetics|June 15, 1993
Transposon-like element in the dystrophin geneM Zatz, M R Passos-Bueno, M Vainzof
Journal of Medical Genetics|July 1, 1993
Facioscapulohumeral muscular dystrophy: aspects of genetic counselling, acceptance of preclinical diagnosis, and fitnessS Eggers, M R Passos-Bueno, M Zatz
Current Opinion in Neurology|November 10, 2000
Limb-girdle muscular dystrophy: one gene with different phenotypes, one phenotype with different genesM Zatz, M Vainzof, M R Passos-Bueno
American Journal of Medical Genetics|May 1, 1983
Serum pyruvate-kinase (PK) activity during pregnancy in potential carriers for Duchenne muscular dystrophyM Zatz, M R Passos, E R Bortolini
Human Mutation|March 27, 1999
A new three allele polymorphism at distal 21q22.3, a region relatively devoid of polymorphic markers. Mutations in brief no. 212. OnlineA L Sertié, C Brahe, M R Passos-Bueno
Pageof 15

Showing results (1-10 of 142) with videos related to

Sort By:
Pageof 15
American Journal of Medical Genetics|November 1, 1983
Creatine-kinase (CK) and pyruvate-kinase (PK) activities in cord blood of normal newborn infants: application to Duchenne muscular dystrophy screening programsM R Passos, M Zatz
Journal of Medical Genetics|April 1, 1991
Reproductive fitness and frequency of new mutations in Becker muscular dystrophy: implications for genetic risk estimatesM R Passos-Bueno, M Zatz
American Journal of Medical Genetics|March 1, 1989
Estimate of the proportion of Duchenne muscular dystrophy with autosomal recessive inheritanceM Zatz, M R Passos-Bueno, D Rapaport
American Journal of Medical Genetics|October 1, 1985
Creatine-kinase and pyruvate-kinase activities in normal children: implications in Duchenne muscular dystrophy carrier detectionM R Passos, C H Gonzalez, M Zatz
American Journal of Medical Genetics|October 1, 1990
Duchenne-like muscular dystrophy in the ArabsM Zatz, M R Passos-Bueno, D Rapaport
American Journal of Medical Genetics|June 15, 1993
Transposon-like element in the dystrophin geneM Zatz, M R Passos-Bueno, M Vainzof
Journal of Medical Genetics|July 1, 1993
Facioscapulohumeral muscular dystrophy: aspects of genetic counselling, acceptance of preclinical diagnosis, and fitnessS Eggers, M R Passos-Bueno, M Zatz
Current Opinion in Neurology|November 10, 2000
Limb-girdle muscular dystrophy: one gene with different phenotypes, one phenotype with different genesM Zatz, M Vainzof, M R Passos-Bueno
American Journal of Medical Genetics|May 1, 1983
Serum pyruvate-kinase (PK) activity during pregnancy in potential carriers for Duchenne muscular dystrophyM Zatz, M R Passos, E R Bortolini
Human Mutation|March 27, 1999
A new three allele polymorphism at distal 21q22.3, a region relatively devoid of polymorphic markers. Mutations in brief no. 212. OnlineA L Sertié, C Brahe, M R Passos-Bueno
Pageof 15