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Association between APOE polymorphisms and predisposition for autism.
Giunco CT, de Oliveira AB, Carvalho-Salles AB, Souza DS, Silva AE, da Rocha SS, Fett-Conte AC. Giunco CT, et al. Psychiatr Genet. 2009 Dec;19(6):338. doi: 10.1097/YPG.0b013e3283328e41. Psychiatr Genet. 2009. PMID: 19859026 No abstract available.
MOMO syndrome associated with autism: a case report.
Giunco CT, Moretti-Ferreira D, Silva AE, Rocha SS, Fett-Conte AC. Giunco CT, et al. Genet Mol Res. 2008 Nov 4;7(4):1223-5. doi: 10.4238/vol7-4gmr522. Genet Mol Res. 2008. PMID: 19048502
Subtelomeric region of chromosome 2 in patients with autism spectrum disorders.
Barbosa-Gonçalves A, Vendrame-Goloni CB, Martins AL, Fett-Conte AC. Barbosa-Gonçalves A, et al. Genet Mol Res. 2008 Jun 17;7(2):527-33. doi: 10.4238/vol7-2gmr448. Genet Mol Res. 2008. PMID: 18752177
Single nucleotide polymorphisms in the CNTNAP2 gene in Brazilian patients with autistic spectrum disorder.
Nascimento PP, Bossolani-Martins AL, Rosan DB, Mattos LC, Brandão-Mattos C, Fett-Conte AC. Nascimento PP, et al. Among authors: fett conte ac. Genet Mol Res. 2016 Feb 5;15(1). doi: 10.4238/gmr.15017422. Genet Mol Res. 2016. PMID: 26909962 Free article.
Acheiropodia: report on four new Brazilian patients.
Fett-Conte AC, Richieri-Costa A. Fett-Conte AC, et al. Am J Med Genet. 1990 Jul;36(3):341-4. doi: 10.1002/ajmg.1320360320. Am J Med Genet. 1990. PMID: 2363435
Clonal monosomy of chromosome 21 in a case of myelodysplastic syndrome.
Freitas PC, Carvalho-Salles AB, Mendiburu CF, Ricci O Jr, Fett-Conte AC. Freitas PC, et al. Genet Mol Res. 2011 Nov 4;10(4):2718-20. doi: 10.4238/2011.November.4.5. Genet Mol Res. 2011. PMID: 22095597
Global gene expression profile in myelodysplastic syndromes using SAGE.
Mendiburu CF, Silva WA Jr, Ricci O Jr, Bonini-Domingos CR, Fett-Conte AC. Mendiburu CF, et al. Genet Mol Res. 2008;7(4):1245-50. doi: 10.4238/vol7-4gmr521. Genet Mol Res. 2008. PMID: 19065759
[Familial Bloom's syndrome associated with neuroblastoma].
Antõnio JR, Fett-Conte AC, Thomé JA, Silva AE, Pozetti EM, Nakaoshi PC, Toledo EC, Leser PG, Solé D, Naspitz CK. Antõnio JR, et al. Rev Paul Med. 1990 Jan-Feb;108(1):9-16. Rev Paul Med. 1990. PMID: 2218304 Portuguese.
Translocation (11;19)(q23;p13.3) associated with a novel t(5;16) (q13;q22) in a patient with acute myelocytic leukemia.
Vendrame-Goloni CB, Varella-Garcia M, Carvalho-Salles AB, Ruiz MA, Júnior OR, Fett-Conte AC. Vendrame-Goloni CB, et al. Cancer Genet Cytogenet. 2003 Feb;141(1):71-4. doi: 10.1016/s0165-4608(02)00646-5. Cancer Genet Cytogenet. 2003. PMID: 12581901
A multicentric association study between 39 genes and nonsyndromic cleft lip and palate in a Brazilian population.
de Araujo TK, Secolin R, Félix TM, de Souza LT, Fontes MÍ, Monlleó IL, de Souza J, Fett-Conte AC, Ribeiro EM, Xavier AC, de Rezende AA, Simioni M, Ribeiro-dos-Santos ÂK, dos Santos SE, Gil-da-Silva-Lopes VL. de Araujo TK, et al. Among authors: fett conte ac. J Craniomaxillofac Surg. 2016 Jan;44(1):16-20. doi: 10.1016/j.jcms.2015.07.026. Epub 2015 Aug 13. J Craniomaxillofac Surg. 2016. PMID: 26602496
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