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M R Passos

Showing results (81-90 of 142) with videos related to

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Neuromuscular Disorders : NMD|January 1, 1991
Dystrophin immunofluorescence pattern in manifesting and asymptomatic carriers of Duchenne's and Becker muscular dystrophies of different agesM Vainzof, R C Pavanello, I Pavanello, et al.
American Journal of Medical Genetics|December 18, 1998
Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriersD R Sumita, M Vainzof, S Campiotto, et al.
Journal of the Neurological Sciences|April 1, 1991
Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy (FSH) at 6q23-q27M R Passos-Bueno, B Byth, D Love, et al.
Genetic Testing|May 4, 2000
Molecular analysis in Brazilian cystic fibrosis patients reveals five novel mutationsA L Bernardino, A Ferri, M R Passos-Bueno, et al.
American Journal of Medical Genetics|February 27, 1995
Why is the reproductive performance lower in Becker (BMD) as compared to limb girdle (LGMD) muscular dystrophy male patients?S Eggers, V Lauriano, M Melo, et al.
Neuromuscular Disorders : NMD|December 1, 1996
The molecular biology of LGMD2B--towards the identification of the LGMD gene on chromosome 2p13K Bushby, R Bashir, S Keers, et al.
American Journal of Medical Genetics|July 24, 1998
Description of a new mutation and characterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostosesM R Passos-Bueno, A L Sertié, A Richieri-Costa, et al.
Neuropediatrics|August 1, 1997
Deficiency of alpha-actinin-3 (ACTN3) occurs in different forms of muscular dystrophyM Vainzof, C S Costa, S K Marie, et al.
American Journal of Medical Genetics|October 26, 1999
Role of the C677T polymorphism at the MTHFR gene on risk to nonsyndromic cleft lip with/without cleft palate: results from a case-control study in BrazilD A Gaspar, R C Pavanello, M Zatz, et al.
American Journal of Medical Genetics|April 18, 1997
The use of apolipoprotein E genotype for preclinical detection of risk's group for Alzheimer's diseaseJ R Oliveira, J L Lima Filho, C M Shimokomaki, et al.
Pageof 15

Showing results (81-90 of 142) with videos related to

Sort By:
Pageof 15
Neuromuscular Disorders : NMD|January 1, 1991
Dystrophin immunofluorescence pattern in manifesting and asymptomatic carriers of Duchenne's and Becker muscular dystrophies of different agesM Vainzof, R C Pavanello, I Pavanello, et al.
American Journal of Medical Genetics|December 18, 1998
Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriersD R Sumita, M Vainzof, S Campiotto, et al.
Journal of the Neurological Sciences|April 1, 1991
Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy (FSH) at 6q23-q27M R Passos-Bueno, B Byth, D Love, et al.
Genetic Testing|May 4, 2000
Molecular analysis in Brazilian cystic fibrosis patients reveals five novel mutationsA L Bernardino, A Ferri, M R Passos-Bueno, et al.
American Journal of Medical Genetics|February 27, 1995
Why is the reproductive performance lower in Becker (BMD) as compared to limb girdle (LGMD) muscular dystrophy male patients?S Eggers, V Lauriano, M Melo, et al.
Neuromuscular Disorders : NMD|December 1, 1996
The molecular biology of LGMD2B--towards the identification of the LGMD gene on chromosome 2p13K Bushby, R Bashir, S Keers, et al.
American Journal of Medical Genetics|July 24, 1998
Description of a new mutation and characterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostosesM R Passos-Bueno, A L Sertié, A Richieri-Costa, et al.
Neuropediatrics|August 1, 1997
Deficiency of alpha-actinin-3 (ACTN3) occurs in different forms of muscular dystrophyM Vainzof, C S Costa, S K Marie, et al.
American Journal of Medical Genetics|October 26, 1999
Role of the C677T polymorphism at the MTHFR gene on risk to nonsyndromic cleft lip with/without cleft palate: results from a case-control study in BrazilD A Gaspar, R C Pavanello, M Zatz, et al.
American Journal of Medical Genetics|April 18, 1997
The use of apolipoprotein E genotype for preclinical detection of risk's group for Alzheimer's diseaseJ R Oliveira, J L Lima Filho, C M Shimokomaki, et al.
Pageof 15