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International Journal of Cardiology
|
October 22, 2008
Determinants of left ventricular mass and presence of metabolic risk factors in normotensive individuals
Sérgio Lamêgo Rodrigues, Lílian C S Angelo, Alexandre C Pereira, et al.
Genetic Testing and Molecular Biomarkers
|
February 9, 2010
Williams-Beuren syndrome: diagnosis by polymorphic markers
Ivanete C Sbruzzi, Alexandre C Pereira, Beatriz Vasconcelos, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 6, 2002
A novel Val648Ile substitution in RET protooncogene observed in a Cys634Arg multiple endocrine neoplasia type 2A kindred presenting with an adrenocorticotropin-producing pheochromocytoma
Adriana B Nunes, Marilza C L Ezabella, Alexandre C Pereira, et al.
International Journal of Cardiology
|
November 25, 2004
High-sensitivity C-reactive protein concentration in a healthy Brazilian population
Fernando Araújo, Alexandre C Pereira, Maria do Rosário D O Latorre, et al.
Genetic Epidemiology
|
March 31, 2016
Bayesian Variable Selection in Multilevel Item Response Theory Models with Application in Genomics
Tiago M Fragoso, Mariza de Andrade, Alexandre C Pereira, et al.
American Journal of Medical Genetics. Part A
|
September 24, 2004
Clinical variability in a Noonan syndrome family with a new PTPN11 gene mutation
Débora Romeo Bertola, Alexandre C Pereira, Paulo S L de Oliveira, et al.
BMC Genetics
|
January 22, 2011
An empirical evaluation of imputation accuracy for association statistics reveals increased type-I error rates in genome-wide associations
Marcio A A Almeida, Paulo S L Oliveira, Tiago V Pereira, et al.
Human Molecular Genetics
|
May 1, 2012
Regulatory variation in a TBX5 enhancer leads to isolated congenital heart disease
Scott Smemo, Luciene C Campos, Ivan P Moskowitz, et al.
American Journal of Human Genetics
|
October 2, 2020
Roadmap for Establishing Large-Scale Genomic Medicine Initiatives in Low- and Middle-Income Countries
George P Patrinos, Emmanouil Pasparakis, Erasmia Koiliari, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
January 22, 2004
Methylenetetrahydrofolate reductase (MTHFR) c677t gene variant modulates the homocysteine folate correlation in a mild folate-deficient population
Alexandre C Pereira, Isolmar Tadeu Schettert, Antônio Alberto F Morandini Filho, et al.
Page
of 35
Search research articles
Search
Showing results (41-50 of 348) with videos related to
Sort By:
Page
of 35
International Journal of Cardiology
|
October 22, 2008
Determinants of left ventricular mass and presence of metabolic risk factors in normotensive individuals
Sérgio Lamêgo Rodrigues, Lílian C S Angelo, Alexandre C Pereira, et al.
Genetic Testing and Molecular Biomarkers
|
February 9, 2010
Williams-Beuren syndrome: diagnosis by polymorphic markers
Ivanete C Sbruzzi, Alexandre C Pereira, Beatriz Vasconcelos, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 6, 2002
A novel Val648Ile substitution in RET protooncogene observed in a Cys634Arg multiple endocrine neoplasia type 2A kindred presenting with an adrenocorticotropin-producing pheochromocytoma
Adriana B Nunes, Marilza C L Ezabella, Alexandre C Pereira, et al.
International Journal of Cardiology
|
November 25, 2004
High-sensitivity C-reactive protein concentration in a healthy Brazilian population
Fernando Araújo, Alexandre C Pereira, Maria do Rosário D O Latorre, et al.
Genetic Epidemiology
|
March 31, 2016
Bayesian Variable Selection in Multilevel Item Response Theory Models with Application in Genomics
Tiago M Fragoso, Mariza de Andrade, Alexandre C Pereira, et al.
American Journal of Medical Genetics. Part A
|
September 24, 2004
Clinical variability in a Noonan syndrome family with a new PTPN11 gene mutation
Débora Romeo Bertola, Alexandre C Pereira, Paulo S L de Oliveira, et al.
BMC Genetics
|
January 22, 2011
An empirical evaluation of imputation accuracy for association statistics reveals increased type-I error rates in genome-wide associations
Marcio A A Almeida, Paulo S L Oliveira, Tiago V Pereira, et al.
Human Molecular Genetics
|
May 1, 2012
Regulatory variation in a TBX5 enhancer leads to isolated congenital heart disease
Scott Smemo, Luciene C Campos, Ivan P Moskowitz, et al.
American Journal of Human Genetics
|
October 2, 2020
Roadmap for Establishing Large-Scale Genomic Medicine Initiatives in Low- and Middle-Income Countries
George P Patrinos, Emmanouil Pasparakis, Erasmia Koiliari, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
January 22, 2004
Methylenetetrahydrofolate reductase (MTHFR) c677t gene variant modulates the homocysteine folate correlation in a mild folate-deficient population
Alexandre C Pereira, Isolmar Tadeu Schettert, Antônio Alberto F Morandini Filho, et al.
Page
of 35