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M R Passos

Showing results (21-30 of 142) with videos related to

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Journal of the Neurological Sciences|July 1, 1995
Is dystrophin always altered in Becker muscular dystrophy patients?M Vainzof, M R Passos-Bueno, R C Pavanello, et al.
Human Molecular Genetics|June 1, 1994
Half the dystrophin gene is apparently enough for a mild clinical course: confirmation of its potential use for gene therapyM R Passos-Bueno, M Vainzof, S K Marie, et al.
American Journal of Medical Genetics|March 1, 1989
Hypothesis: the existence of embryonic and adult isoforms of mRNA dystrophin provides an explanation for unusual clinical findingsM Zatz, M R Passos-Bueno, M Vainzof, et al.
The Journal of Infection|April 13, 2000
Epidemiological aspects of human papillomavirus infection and cervical cancer in BrazilS M Cavalcanti, L G Zardo, M R Passos, et al.
Journal of Medical Genetics|August 27, 1998
Presence of the Apert canonical S252W FGFR2 mutation in a patient without severe syndactylyM R Passos-Bueno, A Richieri-Costa, A L Sertié, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Steroids in Duchenne muscular dystrophyM Zatz, R de C Pavanello, M Vainzof, et al.
American Journal of Medical Genetics|August 8, 1997
Pfeiffer mutation in an Apert patient: how wide is the spectrum of variability due to mutations in the FGFR2 gene?M R Passos-Bueno, A L Sertié, M Zatz, et al.
Human Molecular Genetics|January 1, 1993
Point mutation in a Becker muscular dystrophy patientR G Roberts, M R Passos-Bueno, M Bobrow, et al.
American Journal of Medical Genetics|January 9, 2001
Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasiaP Iughetti, L G Alonso, W Wilcox, et al.
Journal of Medical Genetics|July 1, 1992
A model to estimate the expression of the dystrophin gene in muscle from female Becker muscular dystrophy carriersM Vainzof, M R Passos-Bueno, R C Pavanello, et al.
Pageof 15

Showing results (21-30 of 142) with videos related to

Sort By:
Pageof 15
Journal of the Neurological Sciences|July 1, 1995
Is dystrophin always altered in Becker muscular dystrophy patients?M Vainzof, M R Passos-Bueno, R C Pavanello, et al.
Human Molecular Genetics|June 1, 1994
Half the dystrophin gene is apparently enough for a mild clinical course: confirmation of its potential use for gene therapyM R Passos-Bueno, M Vainzof, S K Marie, et al.
American Journal of Medical Genetics|March 1, 1989
Hypothesis: the existence of embryonic and adult isoforms of mRNA dystrophin provides an explanation for unusual clinical findingsM Zatz, M R Passos-Bueno, M Vainzof, et al.
The Journal of Infection|April 13, 2000
Epidemiological aspects of human papillomavirus infection and cervical cancer in BrazilS M Cavalcanti, L G Zardo, M R Passos, et al.
Journal of Medical Genetics|August 27, 1998
Presence of the Apert canonical S252W FGFR2 mutation in a patient without severe syndactylyM R Passos-Bueno, A Richieri-Costa, A L Sertié, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Steroids in Duchenne muscular dystrophyM Zatz, R de C Pavanello, M Vainzof, et al.
American Journal of Medical Genetics|August 8, 1997
Pfeiffer mutation in an Apert patient: how wide is the spectrum of variability due to mutations in the FGFR2 gene?M R Passos-Bueno, A L Sertié, M Zatz, et al.
Human Molecular Genetics|January 1, 1993
Point mutation in a Becker muscular dystrophy patientR G Roberts, M R Passos-Bueno, M Bobrow, et al.
American Journal of Medical Genetics|January 9, 2001
Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasiaP Iughetti, L G Alonso, W Wilcox, et al.
Journal of Medical Genetics|July 1, 1992
A model to estimate the expression of the dystrophin gene in muscle from female Becker muscular dystrophy carriersM Vainzof, M R Passos-Bueno, R C Pavanello, et al.
Pageof 15