J. K. Heinrich

发表

Genomic imbalances detected through array CGH in fetuses with holoprosencephaly.

R. Barini, I. Machado, J. K. Heinrich, 2011, Arquivos de neuro-psiquiatria.

Copy number imbalances detected with a BAC-based array comparative genomic hybridization platform in congenital diaphragmatic hernia fetuses.

R. Barini, C. Peralta, I. Machado, 2011, Genetics and molecular research : GMR.

Analysis of BRCA1 and BRCA2 mutations in Brazilian breast cancer patients with positive family history.

F. Schmitt, R. Dufloth, S. Carvalho, 2005, Sao Paulo medical journal = Revista paulista de medicina.

The investigation of DNA repair polymorphisms with histopathological characteristics and hormone receptors in a group of Brazilian women with breast cancer.

F. Schmitt, R. Dufloth, L. Zeferino, 2008, Genetics and molecular research : GMR.

Array CGH in Fetal Medicine Diagnosis

R. Barini, J. K. Heinrich, I. N. Machado, 2012 .

HER‐2 and cancer antigen 125 evaluation in ovarian borderline tumors by immunohistochemistry and fluorescence in situ hybridization

M. Varella‐Garcia, L. Andrade, J. K. Heinrich, 2004, International journal of gynecological cancer : official journal of the International Gynecological Cancer Society.

[Subfertility phenotype, chromosome polymorphism and conception failures].

R. Barini, E. Couto, J. K. Heinrich, 2011, Revista brasileira de ginecologia e obstetricia : revista da Federacao Brasileira das Sociedades de Ginecologia e Obstetricia.

Aluminum concentrations in central and peripheral areas of malignant breast lesions do not differ from those in normal breast tissues

L. Sarian, S. Cadore, S. Derchain, 2013, BMC Cancer.

Tissue Aluminum Concentration Does Not Affect the Genomic Stability of ERBB2, C-MYC, and CCND1 Genes in Breast Cancer

L. Sarian, S. Cadore, S. Derchain, 2013, Biological Trace Element Research.

[ErbB-2 expression and hormone receptor status in areas of transition from in situ to invasive ductal breast carcinoma].

L. Sarian, F. Soares, S. Derchain, 2009, Revista brasileira de ginecologia e obstetricia : revista da Federacao Brasileira das Sociedades de Ginecologia e Obstetricia.

Non‐immune hydrops fetalis: A prospective study of 53 cases

D. Cavalcanti, R. Giugliani, R. Barini, 2013, American journal of medical genetics. Part A.

Comparative evaluation of the erbB2 and hormone receptor status of neighboring invasive and in situ components of ductal carcinomas of the breast

J. H. Yoon, L. Sarian, I. D. da Cunha, 2009 .

Comparative evaluation of the erbB2 and hormone receptor status of neighboring invasive and in situ components of ductal carcinomas of the breast.

J. H. Yoon, L. Sarian, I. D. da Cunha, 2009, The International journal of biological markers.

Reduced Prevalence of the C825T Polymorphism of the G-Protein Beta Subunit Gene in Women with Breast Cancer

L. Sarian, R. Paleari, S. Derchain, 2011, International Journal of Biological Markers.

Prenatal diagnosis of a partial trisomy 13q (q14-->qter): phenotype, cytogenetics and molecular characterization by spectral karyotyping and array comparative genomic hybridization.

I N Machado, J K Heinrich, C Campanhol, 2010, Genetics and molecular research : GMR.

Prenatal Genomic Profiling of Abdominal Wall Defects through Comparative Genomic Hybridization: Perspectives for a New Diagnostic Tool

R. Barini, L. Sbragia, J. K. Heinrich, 2007, Fetal Diagnosis and Therapy.

Characterization of cells recovered from the xenotransplanted NG97 human-derived glioma cell line subcultured in a long-term in vitro

W. Savino, L. Verinaud, A. Schenka, 2008, BMC Cancer.