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Ana Peixoto

Showing results (1-10 of 80) with videos related to

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Acta Medica Portuguesa|February 3, 2024
[Letter to the Editor Regarding "Prevalence and Predictive Factors of Exclusive Breastfeeding in the First Six Months of Life"]Ana Peixoto
The International Journal of Esthetic Dentistry|January 23, 2016
Gingival biotype characterization--a study in a Portuguese sampleAna Peixoto, Tiago M Marques, André Correia
Expert Reviews in Molecular Medicine|December 19, 2018
Potential clinical applications of circulating cell-free DNA in ovarian cancer patientsAna Barbosa, Ana Peixoto, Pedro Pinto, et al.
Breast Cancer Research and Treatment|October 15, 2008
Molecular diagnosis of the Portuguese founder mutation BRCA2 c.156_157insAluAna Peixoto, Catarina Santos, Patrícia Rocha, et al.
Plos Genetics|April 17, 2018
Targeted next generation sequencing identifies functionally deleterious germline mutations in novel genes in early-onset/familial prostate cancerPaula Paulo, Sofia Maia, Carla Pinto, et al.
Journal of Cutaneous Pathology|March 1, 2011
Intraepidermal epidermotropic metastatic melanoma: a clinical and histopathological mimicker of melanoma in situ occurring in multiplicitySara Lestre, Alexandre João, Pedro Ponte, et al.
Cancer Genetics and Cytogenetics|September 25, 2007
Molecular characterization of a rare MLL-AF4 (MLL-AFF1) fusion rearrangement in infant leukemiaSusana Bizarro, Nuno Cerveira, Cecília Correia, et al.
Neoplasia (New York, N.Y.)|October 13, 2006
TMPRSS2-ERG gene fusion causing ERG overexpression precedes chromosome copy number changes in prostate carcinomas and paired HGPIN lesionsNuno Cerveira, Franclim R Ribeiro, Ana Peixoto, et al.
Journal of Human Genetics|December 11, 2012
Genomic characterization of two large Alu-mediated rearrangements of the BRCA1 geneAna Peixoto, Manuela Pinheiro, Lígia Massena, et al.
American Journal of Medical Genetics. Part A|June 25, 2004
A new insight into fragile X syndrome among Basque populationOlga Peñagarikano, Alberto Gil, Mercedes Télez, et al.
Pageof 8

Showing results (1-10 of 80) with videos related to

Sort By:
Pageof 8
Acta Medica Portuguesa|February 3, 2024
[Letter to the Editor Regarding "Prevalence and Predictive Factors of Exclusive Breastfeeding in the First Six Months of Life"]Ana Peixoto
The International Journal of Esthetic Dentistry|January 23, 2016
Gingival biotype characterization--a study in a Portuguese sampleAna Peixoto, Tiago M Marques, André Correia
Expert Reviews in Molecular Medicine|December 19, 2018
Potential clinical applications of circulating cell-free DNA in ovarian cancer patientsAna Barbosa, Ana Peixoto, Pedro Pinto, et al.
Breast Cancer Research and Treatment|October 15, 2008
Molecular diagnosis of the Portuguese founder mutation BRCA2 c.156_157insAluAna Peixoto, Catarina Santos, Patrícia Rocha, et al.
Plos Genetics|April 17, 2018
Targeted next generation sequencing identifies functionally deleterious germline mutations in novel genes in early-onset/familial prostate cancerPaula Paulo, Sofia Maia, Carla Pinto, et al.
Journal of Cutaneous Pathology|March 1, 2011
Intraepidermal epidermotropic metastatic melanoma: a clinical and histopathological mimicker of melanoma in situ occurring in multiplicitySara Lestre, Alexandre João, Pedro Ponte, et al.
Cancer Genetics and Cytogenetics|September 25, 2007
Molecular characterization of a rare MLL-AF4 (MLL-AFF1) fusion rearrangement in infant leukemiaSusana Bizarro, Nuno Cerveira, Cecília Correia, et al.
Neoplasia (New York, N.Y.)|October 13, 2006
TMPRSS2-ERG gene fusion causing ERG overexpression precedes chromosome copy number changes in prostate carcinomas and paired HGPIN lesionsNuno Cerveira, Franclim R Ribeiro, Ana Peixoto, et al.
Journal of Human Genetics|December 11, 2012
Genomic characterization of two large Alu-mediated rearrangements of the BRCA1 geneAna Peixoto, Manuela Pinheiro, Lígia Massena, et al.
American Journal of Medical Genetics. Part A|June 25, 2004
A new insight into fragile X syndrome among Basque populationOlga Peñagarikano, Alberto Gil, Mercedes Télez, et al.
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