Centro de Biologia Molecular e Engenharia Genética   Produções / Resumos Publicados Resumos publicados em anais de congressos (internacional)   1.   MELLO, Maricilda Palandi; SOARDI, F. C.; LEMOS-MARINI, Sofia Helena Valente; GUERRA JUNIOR, Gil; BAPTISTA, Maria Tereza Matias; "Congenital Adrena Hyperplasia: Novel Mutations in the CYP21 Gene", 09/2002, 41st. Annual Meeting of The European Society for Paediatric Endocrinology, Vol. 58, pp.45-45, Madrid, ESPANHA, 2002   2.   GUERRA JUNIOR, Gil; DANTAS NASCIMENTO, sandra regina; ARAÚJO, Marcela; CONDINO NETO, Antonio; LEMOS-MARINI, Sofia Helena Valente; MELLO, Maricilda Palandi; "Congenital adrenal hyperplasia due to classic 21 hydroxylase (CYP21) deficiency: possible association with C4 deficiency", 09/2002, XIX International Complement Workshop, Vol. 2, pp.1380-1381, Palermo, ITALIA, 2002   3.   OTTOBONI, Laura M.M.; BERGAMO, Rogério F.; "Differentiation of Acidithiobacillus ferrooxidans and A. thiooxidans by RFLP and sequence analysis of the 16S-23S rDNA spacer region", 08/2002, Society for Industrial Microbiology Annual Meeting, Vol. 53, pp.106-106, Filadelfia, ESTADOS UNIDOS, 2002   4.   ASSMANN, ELIANA MARIA; OTTOBONI, Laura M.M.; FERRAZ, André; RODRIGUEZ, Jaime; MELLO, Maricilda Palandi; "Differential display used for isolation of Phanerochaete chrysosporium mRNAs induced by different iron growth conditions", 08/2002, Society for Industrial Microbiology Annual Meeting, Vol. 53, pp.106-106, Filadelfia, ESTADOS UNIDOS, 2002   5.   GUERRA JUNIOR, Gil; DANTAS NASCIMENTO, sandra regina; ARAÚJO, Marcela; CONDINO NETO, Antonio; LEMOS-MARINI, Sofia Helena Valente; MELLO, Maricilda Palandi; "Congenital Adrenal Hyperplasia due to Classic 21-Hydroxylase (CYP21) Deficiency: Possible Association with C4 Deficilncy", 08/2002, VIII ENCONTRO DO GRUPO LATINO-AMERICANO DE IMUNODEFICIÊNCIAS PRIMÉRIAS E II ENCONTRO DO GRUPO BRASILEIRO DE IMUNODEFICIÊNCIAS, Vol. 10, pp.28-28, Campinas, SP, BRASIL, 2002   6.   GUERRA JUNIOR, Gil; DANTAS NASCIMENTO, sandra regina; ARAÚJO, Marcela; CONDINO NETO, Antonio; LEMOS-MARINI, Sofia Helena Valente; MELLO, Maricilda Palandi; "Congenital Adrenal Hyperplasia due to classic 3 b hydroxysteroid dehydrogenase deficiency associated with low serum C4 levels and molecular alteration on C4 genes", 08/2002, XIX International Complement Workshop, Vol. 2, pp.1383-1383, Palermo, ITALIA, 2002   7.   CASTRO, M; PENACHIONI, JY; SARTORI SANCHEZ BACHEGA, Tania Aparecida; MELLO, Maricilda Palandi; "Mutations in the CYP11B1 in Brazilian patients with 11b-Hydroxylase Deficiency", 06/2002, 84th Annual Meeting of the Endocrine Society, Vol. 84, pp.315-315, São Francisco, ESTADOS UNIDOS, 2002   8.   MELLO, Maricilda Palandi; SOARDI, F. C.; LEMOS-MARINI, Sofia Helena Valente; GUERRA JUNIOR, Gil; BAPTISTA, Maria Tereza Matias; "Three novel mutations in the CYP21 gene in patients with the classical form of congenital 21-hydroxylase deficiency", 05/2002, European Human Genetics Conference 2002, Vol. 10, pp.207-207, Strasbourg, FRANCA, 2002   9.   BAPTISTA, Maria Tereza Matias; ASSUMPÇÃO, Juliana Godoy; GUERRA, Andrea Trevas Maciel; SCOLFARO, Márcia Ribeiro; MELLO, Maricilda Palandi; GUERRA JUNIOR, Gil; "A Family with Different Phenotypes of Gonadal Dysgenesis Associated with the Same Mutation on the SRY Gene", 05/2002, 41th Annual Meeting for the European Society for Pediatric Endocrinology., Vol. 58, pp.139-139, Madrid, ESPANHA, 2002   10.   ASSUMPÇÃO, Juliana G.; GUERRA, Andrea Trevas Maciel; MARQUES DE FARIA, Antonia Paula; MELLO, Maricilda Palandi; "An inherited three base pair deletion in a Sp1-binding site in the 5'non-coding region of SRY gene is associated with sex reversal", 05/2002, European Human Genetics Conference 2002, Vol. 10, pp.303-303, Strasbourg, FRANCA, 2002   11.   SARTORATO, Edi Lúcia; "Clinical heterogenity in a family with M34T variant in the GJB2 gene", 01/2002, European Human Genetics Conference 2002, Vol. 10, pp.248-248, Strasbourg, FRANCA, 2002   12.   SARTORATO, Edi Lúcia; "Clinical heterogenity in a family with M34T variant in the GJB2 gene", 01/2002, European Human Genetics Conference 2002, Vol. 10, pp.248-248, Strasbourg, FRANCA, 2002   13.   REIS, FERNANDA DE CASTRO; NORATO, Denise Yvonne J; CAVALCANTI, Denise Pontes; SARTORATO, Edi Lúcia; "Aplicação das técnicas de biologia molecular no diagnóstico da osteogênese imperfeita", 01/2002, 5 Congresso Internacional de Osteoporose e Metabilismo Mineral, Vol. 1, pp.1-1, Vitória, ES, BRASIL, 2002