Publications

Found 7 results
Filters: Author is A.C. Fett-Conte  [Clear All Filters]
2016
P. P. Nascimento, Bossolani-Martins, A. L., Rosan, D. B. A., Mattos, L. C., Brandão-Mattos, C., Fett-Conte, A. C., Nascimento, P. P., Bossolani-Martins, A. L., Rosan, D. B. A., Mattos, L. C., Brandão-Mattos, C., and Fett-Conte, A. C., “Single nucleotide polymorphisms in the CNTNAP2 gene in Brazilian patients with autistic spectrum disorder”, vol. 15, p. -, 2016.
P. P. Nascimento, Bossolani-Martins, A. L., Rosan, D. B. A., Mattos, L. C., Brandão-Mattos, C., Fett-Conte, A. C., Nascimento, P. P., Bossolani-Martins, A. L., Rosan, D. B. A., Mattos, L. C., Brandão-Mattos, C., and Fett-Conte, A. C., “Single nucleotide polymorphisms in the CNTNAP2 gene in Brazilian patients with autistic spectrum disorder”, vol. 15, p. -, 2016.
2011
P. C. Freitas, Carvalho-Salles, A. B., Mendiburu, C. F., Ricci, Jr., O., and Fett-Conte, A. C., “Clonal monosomy of chromosome 21 in a case of myelodysplastic syndrome”, vol. 10. pp. 2718-2720, 2011.
Haase D (2008). Cytogenetic features in myelodysplastic syndromes. Ann. Hematol. 87: 515-526.http://dx.doi.org/10.1007/s00277-008-0483-yPMid:18414863    PMCid:2413090Haase D, Germing U, Schanz J, Pfeilstocker M, et al. (2007). New insights into the prognostic impact of the karyotype in MDS and correlation with subtypes: evidence from a core dataset of 2124 patients. Blood 110: 4385-4395.http://dx.doi.org/10.1182/blood-2007-03-082404PMid:17726160Jadersten M and Hellstrom-Lindberg E (2009). Myelodysplastic syndromes: biology and treatment. J. Intern. Med. 265: 307-328.http://dx.doi.org/10.1111/j.1365-2796.2008.02052.xPMid:19141095Malcovati L and Nimer SD (2008). Myelodysplastic syndromes: diagnosis and staging. Cancer Control 15: 4-13.Mufti GJ, Bennett JM, Goasguen J, Bain BJ, et al. (2008). Diagnosis and classification of myelodysplastic syndrome: international working group on morphology of myelodysplastic syndrome (IWGM-MDS) consensus proposals for the definition and enumeration of myeloblasts and ring sideroblasts. Haematologica 93: 1712-1717.http://dx.doi.org/10.3324/haematol.13405PMid:18838480Shaffer LG and Tommerup N (2009). An International System for Human Cytogenetic Nomenclature ISCN. ND-S Karger Publishers Inc., Basel.Wang H, Wang XQ, Xu XP and Lin GW (2010). Cytogenetic evolution correlates with poor prognosis in myelodysplastic syndrome. Cancer Genet. Cytogenet. 196: 159-166.http://dx.doi.org/10.1016/j.cancergencyto.2009.09.015PMid:20082852
2008
C. B. Vendrame-Goloni, Carvalho-Salles, A. B., Ruiz, M. A., O. Júnior, R., Varella-Garcia, M., and Fett-Conte, A. C., “Clinical outcome in chronic myeloid leukemia after allogeneic hematopoietic stem cell transplantation: the experience of the Bone Marrow Transplantation Unit of FUNFARME/BRAZIL using FISH”, vol. 7, pp. 417-423, 2008.
C. F. Mendiburu, Silva, Jr, W. A., Ricci, Jr., O., Bonini-Domingos, C. R., and Fett-Conte, A. C., “Global gene expression profile in myelodysplastic syndromes using SAGE”, vol. 7, pp. 1245-1250, 2008.
C. T. Giunco, Moretti-Ferreira, D., Silva, A. E., Rocha, S. S., and Fett-Conte, A. C., “MOMO syndrome associated with autism: a case report”, vol. 7. pp. 1223-1225, 2008.
A. Barbosa-Gonçalves, Vendrame-Goloni, C. B., Martins, A. L. B., and Fett-Conte, A. C., “Subtelomeric region of chromosome 2 in patients with autism spectrum disorders”, vol. 7, pp. 527-533, 2008.