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CBMEG - Resumos em periódicos especializados
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Centro de Biologia Molecular e Engenharia Genética
Produções / Resumos Publicados
Resumos em periódicos especializados
Internacional
1.
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BRANDÃO, M.M.; SAAD, Sara T. Olalla; Screening of genetic variants in familial cases of myeloid neoplasms by exome sequencing, 11/2016, Revista Brasileira de Hematologia e Hemoterapia,Vol. 38, Fac. 1, pp.197-197, São Jose do Rio Preto, SP, Brasil, 2016 *
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2.
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ANDRADE, J. G. R.; FABBRI, H. C.; HOLL-ULRICH, K.; WERNER, R; MARQUES DE FARIA, A P; DE MELLO, Maricilda Palandi; GUERRA JUNIOR, Gil; MACIEL-GUERRA, AT; HIORT, Olaf; Histological Features in Partial and Mixed Gonadal Dysgenesis Biopsy and Gonadectomy Material: Review of 43 Cases, 10/2016, Hormone Research in Paediatrics,Vol. 86, pp.22-22, Basel, Suiça, 2016 *
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3.
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ANDRADE, J. G. R.; WERNER, R.; FABBRI, H. C.; GUERRA JUNIOR, Gil; MACIEL-GUERRA, AT; DE MELLO, Maricilda Palandi; HOLL-ULRICH, K.; HIORT, Olaf; HISTOLOGICAL EVALUATION OF PATIENTS WITH PARTIAL GONADAL DYSGENESIS AND NR5A1 MUTATIONS: REVIEW IN LEYDIG AND GERM CELL PATTERN, 09/2016, Archives of Endocrinology and Metabolism (Impresso),Vol. 60, pp.529-529, São Paulo, SP, Brasil, 2016 *
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4.
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ANDRADE, J. G. R.; FABBRI, H. C.; HOLL-ULRICH, K.; WERNER, R.; MARQUES DE FARIA, A P; DE MELLO, Maricilda Palandi; GUERRA JUNIOR, Gil; MACIEL-GUERRA, AT; HISTOLOGICAL FEATURES IN PARTIAL AND MIXED GONADAL DYSGENESIS BIOPSY AND GONADECTOMY MATERIAL: REVIEW OF 43 CASES, 09/2016, Archives of Endocrinology and Metabolism (Impresso),Vol. 60, pp.529-529, São Paulo, SP, Brasil, 2016 *
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5.
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ANDRADE, J. G. R.; FABBRI, H. C.; SANTOS, A. P.; MARQUES DE FARIA, A P; DE MELLO, Maricilda Palandi; GUERRA JUNIOR, Gil; MACIEL-GUERRA, AT; PARTIAL AND MIXED GONADAL DYSGENESIS CANNOT BE DISTINGUISHED BY HISTOLOGICAL PICTURE: CLINICAL EVALUATION, HISTOLOGICAL DIFFERENCES AND LONG TERM FOLLOW UP OF 61 BRAZILIAN PATIENTS, 09/2016, Archives of Endocrinology and Metabolism (Impresso),Vol. 60, pp.30-30, São Paulo, SP, Brasil, 2016 *
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6.
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HENRIQUE, P. P.; CARVALHO, C. R. L.; DE MELLO, Maricilda Palandi; MARQUES DE FARIA, A P; Screening for copy number variations on the X chromosome in patients with unexplained intellectual disability, 05/2016, European Journal of Human Genetics,Vol. 24, pp.439-439, Basingstoke, Reino Unido, 2016 *
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7.
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MACIEL-GUERRA, AT; GUARAGNA, M. S.; GERVASIO DE BRITTO, Anna Cristina; BELANGERO, Vera Maria Santoro; GUERRA JUNIOR, Gil; PRATES, L; Whole exome sequencing identifies a novel mutation in ACTN4 gene in a Brazilian patient with steroid resistant nephrotic syndrome, 05/2016, European Journal of Human Genetics,Vol. 24, pp.90-91, Basingstoke, Reino Unido, 2016 *
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* Esta produção está associada também a outros órgãos
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