10 results for author:"Maciel-Guerra A.T." in Literature citations
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| Multifunctional role of steroidogenic factor 1 and disorders of sex development. Mello M.P., Franca E.S., Fabbri H.C., Maciel-Guerra A.T., Guerra-Junior G. Arq Bras Endocrinol Metabol 55:607-612(2011) · Mapped (6) |
| Mutations in NR5A1 associated with ovarian insufficiency. Lourenco D., Brauner R., Lin L., De Perdigo A., Weryha G., Muresan M., Boudjenah R., Guerra-Junior G., Maciel-Guerra A.T., Achermann J.C. et al. N. Engl. J. Med. 360:1200-1210(2009) · UniProtKB (1) · Mapped (5) |
| XX Maleness and XX true hermaphroditism in SRY-negative monozygotic twins: additional evidence for a common origin. Maciel-Guerra A.T., de Mello M.P., Coeli F.B., Ribeiro M.L., Miranda M.L., Marques-de-Faria A.P., Baptista M.T., Moraes S.G., Guerra-Junior G. J. Clin. Endocrinol. Metab. 93:339-343(2008) · Mapped (19) |
| Allelic frequencies of the 35delG mutation of the GJB2 gene in different Brazilian regions. Oliveira C.A., Pimpinati C.J., Alexandrino F., Magna L.A., Maciel-Guerra A.T., Sartorato E.L. Genet. Test. 11:1-3(2007) · Mapped (3) |
| Frequency of the 35delG mutation in the GJB2 gene in samples of European, Asian, and African Brazilians. Oliveira C.A., Alexandrino F., Abe-Sandes K., Silva W.A. Jr., Maciel-Guerra A.T., Magna L.A., Sartorato E.L. Hum. Biol. 76:313-316(2004) · Mapped (3) |
| Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter study. Del Castillo I., Moreno-Pelayo M.A., Del Castillo F.J., Brownstein Z., Marlin S., Adina Q., Cockburn D.J., Pandya A., Siemering K.R., Chamberlin G.P. et al. Am. J. Hum. Genet. 73:1452-1458(2003) · Mapped (1) |
| Novel mutations affecting SRY DNA-binding activity: the HMG box N65H associated with 46,XY pure gonadal dysgenesis and the familial non-HMG box R30I associated with variable phenotypes. Assumpcao J.G., Benedetti C.E., Maciel-Guerra A.T., Guerra G. Jr., Baptista M.T., Scolfaro M.R., de Mello M.P. J. Mol. Med. 80:782-790(2002) · Mapped (19) |
| Deafness resulting from mutations in the GJB2 (connexin 26) gene in Brazilian patients. Oliveira C.A., Maciel-Guerra A.T., Sartorato E.L. Clin. Genet. 61:354-358(2002) · Mapped (3) |
| Determination of the frequency of the 35delG allele in Brazilian neonates. Sartorato E.L., Gottardi E., de Oliveira C.A., Magna L.A., Annichino-Bizzacchi J.M., Seixas C.A., Maciel-Guerra A.T. Clin. Genet. 58:339-340(2000) · Mapped (3) |
| Mutations of androgen receptor gene in Brazilian patients with male pseudohermaphroditism. Cabral D.F., Maciel-Guerra A.T., Hackel C. Braz. J. Med. Biol. Res. 31:775-778(1998) · UniProtKB (1) |