Browsing by Author Maciel-Guerra, AT

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PreviewIssue DateTitleAuthor(s)AdvisorType
2004Frequency of the 35delG mutation in the GJB2 gene in samples of European, Asian, and African BraziliansOliveira, CA; Alexandrino, E; Abe-Sandes, K; Silva, WA; Maciel-Guerra, AT; Magna, LA; Sartorato, EL-Artigo de periódico
2008XX maleness and XX true hermaphroditism in SRY-negative monozygotic twins: Additional evidence for a common originMaciel-Guerra, AT; de Mello, MP; Coeli, FB; Ribeiro, ML; Miranda, ML; Marques-De-Faria, AP; Baptista, MTM; Moraes, SGE; Guerra-Junior, G-Artigo de periódico
2011Social skills in women with Turner SyndromeSuzigan, LZ; Silva, RBDE; Guerra, G; Marini, SHVL; Maciel-Guerra, AT-Artigo de periódico
2005A naturally occurring deletion in the SRY promoter region affecting the Sp1 binding site is associated with sex reversalAssumpcao, JG; Ferraz, LFC; Benedetti, CE; Maciel-Guerra, AT; Guerra, G; Marques-de-Faria, AP; Baptista, TM; de Mello, MP-Artigo de periódico
2003Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter studydel Castillo, I; Moreno-Pelayo, MA; del Castillo, FJ; Brownstein, Z; Marlin, S; Adina, Q; Cockburn, DJ; Pandya, A; Siemering, KR; Chamberlin, GP; Ballana, E; Wuyts, W; Maciel-Guerra, AT; Alvarez, A; Villamar, M; Shohat, M; Abeliovich, D; Dahl, HHM; Estivill, X; Gasparini, P; Hutchin, T; Nance, WE; Sartorato, EL; Smith, RJH; Van Camp, G; Avraham, KB; Petit, C; Moreno, F-Artigo de periódico
2002Deafness resulting from mutations in the GJB2 (connexin 26) gene in Brazilian patientsOliveira, CA; Maciel-Guerra, AT; Sartorato, EL-Artigo de periódico
2000Evaluation of the tubular and interstitial functions of the testis in 46,XY patients with ambiguous genitaliaStuchi-Perez, EG; Lukas-Croisier, C; De Castro, M; Baptista, MTM; Scolfaro, MR; Marques-De-Faria, AP; Hackel, C; Maciel-Guerra, AT; Guerra, G-Artigo de periódico
1999New frameshift mutation in the 5 alpha-reductase type 2 gene in a Brazilian patient with 5 alpha-reductase deficiencyFerraz, LFC; Baptista, MTM; Maciel-Guerra, AT; Junior, GG; Hackel, C-Artigo de periódico
2010Leber's hereditary optic neuropathy: Clinical and molecular profile of a Brazilian sampleMaciel-Guerra, AT; Zanchetta, LM; Fernandes, MSA; Andrade, PB; Miranda, PMDD; Sartorato, EL-Artigo de periódico
2009Mutations in NR5A1 Associated with Ovarian InsufficiencyLourenco, D; Brauner, R; Lin, L; De Perdigo, A; Weryha, G; Muresan, M; Boudjenah, R; Guerra, G; Maciel-Guerra, AT; Achermann, JC; McElreavey, K; Bashamboo, A-Artigo de periódico
2002Novel 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 phenotypesAssumpcao, JG; Benedetti, CE; Maciel-Guerra, AT; Guerra, G; Baptista, MTM; Scolfaro, MR; de Mello, MP-Artigo de periódico
2005Idiopathic male pseudohermaphroditism is associated with prenatal growth retardationNeto, FDM; Morcillo, AM; Maciel-Guerra, AT; Guerra, G-Artigo de periódico
2002Identification of a neocentromere in a rearranged Y chromosome with no detectable DYZ3 centromeric sequenceAssumpcao, JG; Berkofsky-Fessler, W; Campos, NV; Maciel-Guerra, AT; Li, SL; Melaragno, MI; de Mello, MP; Warburton, PE-Artigo de periódico
1998True hermaphrodites in the southeastern region of Brazil: A different cytogenetic and gonadal profileGuerra, G; de Mello, NP; Assumpcao, JG; Morcillo, AM; Marini, SHVD; Baptista, MTM; Silva, RBPE; Marques-de-Faria, AP; Maciel-Guerra, AT-Artigo de periódico
2012Turner syndrome and metabolic derangements: Another example of fetal programmingBaldin, AD; Siviero-Miachon, AA; Fabbri, T; de Lemos-Marini, SHV; Spinola-Castro, AM; Baptista, MTM; D'Souza-Li, LFR; Morcillo, AM; Maciel-Guerra, AT; Guerra, G-Artigo de periódico
2009Turner's Syndrome and Subclinical Autoimmune Thyroid Disease: A Two-Year Follow-up StudyMedeiros, CCM; de Lemos-Marini, SHV; Bricola, M; Camargo, EE; Santos, AO; Magna, LA; Guerra, G; Baptista, MTM; Maciel-Guerra, AT-Artigo de periódico
2000Turner's syndrome and thyroid disease: A transverse study of pediatric patients in BrazilMedeiros, CCM; Marini, SHVD; Baptista, MTM; Guerra, G; Maciel-Guerra, AT-Artigo de periódico
2007Allelic frequencies of the 35delG mutation of the GJB2 gene in different Brazilian regionsOliveira, CA; Pimpinati, CJ; Alexandrino, F; Magna, LA; Maciel-Guerra, AT; Sartorato, EL-Artigo de periódico
2002Bone mineralization in Turner syndrome: a transverse study of the determinant factors in 58 patientsCosta, AMG; Lemos-Marini, SHV; Baptista, MTM; Morcillo, AM; Maciel-Guerra, AT; Guerra, G-Artigo de periódico
2007Spontaneous final height in Turner's syndrome in Brazilde Lemos-Marini, SHV; Morcillo, AM; Matias Baptista, MT; Guerra, G; Maciel-Guerra, AT-Artigo de periódico