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P A Otto

Showing results (41-50 of 57) with videos related to

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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 Toxicology and Environmental Health|November 1, 1975
A study of chromosomes of lymphocytes from patients treated with hycanthoneO Frota-Pessoa, N R Ferreira, M B Pedroso, et al.
Genetic Epidemiology|November 15, 2002
Evidence that BCL3 plays a role in the etiology of nonsyndromic oral clefts in Brazilian familiesD A Gaspar, S R Matioli, R C Pavanello, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|May 9, 2001
No evidence of association between the D10S1423 locus and Alzheimer disease in Brazilian patientsA L Nishimura, J R Oliveira, P A Otto, et al.
Molecular Psychiatry|October 17, 1998
The short variant of the polymorphism within the promoter region of the serotonin transporter gene is a risk factor for late onset Alzheimer's diseaseJ R Oliveira, R M Gallindo, L G Maia, et al.
Biochemical and Biophysical Research Communications|April 1, 2006
Correspondence regarding Ballana et al., "Mitochondrial 12S rRNA gene mutations affect RNA secondary structure and lead to variable penetrance in hearing impairment"R S Abreu-Silva, A C Batissoco, K Lezirovitz, et al.
Clinical Genetics|January 23, 2009
A novel autosomal dominant deafness locus (DFNA58) maps to 2p12-p21K Lezirovitz, M C C Braga, R S Thiele-Aguiar, et al.
Molecular Syndromology|October 30, 2010
An Illustrative Case of Neurofibromatosis Type 1 and NF1 MicrodeletionL A Praxedes, F M Pereira, J F Mazzeu, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|February 14, 2006
Prevalence of the A1555G (12S rRNA) and tRNASer(UCN) mitochondrial mutations in hearing-impaired Brazilian patientsR S Abreu-Silva, K Lezirovitz, M C C Braga, et al.
American Journal of Medical Genetics|May 29, 1998
Analysis of a novel functional polymorphism within the promoter region of the serotonin transporter gene (5-HTT) in Brazilian patients affected by bipolar disorder and schizophreniaJ R Mendes de Oliveira, P A Otto, H Vallada, et al.
Pageof 6

Showing results (41-50 of 57) with videos related to

Sort By:
Pageof 6
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 Toxicology and Environmental Health|November 1, 1975
A study of chromosomes of lymphocytes from patients treated with hycanthoneO Frota-Pessoa, N R Ferreira, M B Pedroso, et al.
Genetic Epidemiology|November 15, 2002
Evidence that BCL3 plays a role in the etiology of nonsyndromic oral clefts in Brazilian familiesD A Gaspar, S R Matioli, R C Pavanello, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|May 9, 2001
No evidence of association between the D10S1423 locus and Alzheimer disease in Brazilian patientsA L Nishimura, J R Oliveira, P A Otto, et al.
Molecular Psychiatry|October 17, 1998
The short variant of the polymorphism within the promoter region of the serotonin transporter gene is a risk factor for late onset Alzheimer's diseaseJ R Oliveira, R M Gallindo, L G Maia, et al.
Biochemical and Biophysical Research Communications|April 1, 2006
Correspondence regarding Ballana et al., "Mitochondrial 12S rRNA gene mutations affect RNA secondary structure and lead to variable penetrance in hearing impairment"R S Abreu-Silva, A C Batissoco, K Lezirovitz, et al.
Clinical Genetics|January 23, 2009
A novel autosomal dominant deafness locus (DFNA58) maps to 2p12-p21K Lezirovitz, M C C Braga, R S Thiele-Aguiar, et al.
Molecular Syndromology|October 30, 2010
An Illustrative Case of Neurofibromatosis Type 1 and NF1 MicrodeletionL A Praxedes, F M Pereira, J F Mazzeu, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|February 14, 2006
Prevalence of the A1555G (12S rRNA) and tRNASer(UCN) mitochondrial mutations in hearing-impaired Brazilian patientsR S Abreu-Silva, K Lezirovitz, M C C Braga, et al.
American Journal of Medical Genetics|May 29, 1998
Analysis of a novel functional polymorphism within the promoter region of the serotonin transporter gene (5-HTT) in Brazilian patients affected by bipolar disorder and schizophreniaJ R Mendes de Oliveira, P A Otto, H Vallada, et al.
Pageof 6