Alexandrino F - Search Results

1

G59S mutation in the GJB2 (connexin 26) gene in a patient with Bart-Pumphrey syndrome.

Alexandrino F, Sartorato EL, Marques-de-Faria AP, Steiner CE. Alexandrino F, et al. Am J Med Genet A. 2005 Jul 30;136(3):282-4. doi: 10.1002/ajmg.a.30822. Am J Med Genet A. 2005. PMID: 15952212 No abstract available.

2

Molecular genetics study of deafness in Brazil: 8-year experience.

de Oliveira CA, Alexandrino F, Christiani TV, Steiner CE, Cunha JL, Guerra AT, Sartorato EL. de Oliveira CA, et al. Among authors: alexandrino f. Am J Med Genet A. 2007 Jul 15;143A(14):1574-9. doi: 10.1002/ajmg.a.31838. Am J Med Genet A. 2007. PMID: 17567887

3

Molecular study in Brazilian cochlear implant recipients.

Christiani TV, Alexandrino F, de Oliveira CA, Amantini RC, Bevilacqua MC, Filho OA, Porto P, Sartorato EL. Christiani TV, et al. Among authors: alexandrino f. Am J Med Genet A. 2007 Jul 15;143A(14):1580-2. doi: 10.1002/ajmg.a.31778. Am J Med Genet A. 2007. PMID: 17567889

4

Type II autosomal recessive cutis laxa: report of another patient and molecular studies concerning three candidate genes.

Scherrer DZ, Alexandrino F, Cintra ML, Sartorato EL, Steiner CE. Scherrer DZ, et al. Among authors: alexandrino f. Am J Med Genet A. 2008 Nov 1;146A(21):2740-5. doi: 10.1002/ajmg.a.32345. Am J Med Genet A. 2008. PMID: 18819152

5

Connexin mutations in Brazilian patients with skin disorders with or without hearing loss.

Alexandrino F, de Oliveira CA, Magalhães RF, Florence ME, de Souza EM, Sartorato EL. Alexandrino F, et al. Am J Med Genet A. 2009 Feb 15;149A(4):681-4. doi: 10.1002/ajmg.a.32765. Am J Med Genet A. 2009. PMID: 19283857

6

Screening for mutations in the GJB3 gene in Brazilian patients with nonsyndromic deafness.

Alexandrino F, Oliveira CA, Reis FC, Maciel-Guerra AT, Sartorato EL. Alexandrino F, et al. J Appl Genet. 2004;45(2):249-54. J Appl Genet. 2004. PMID: 15131355

7

Allelic frequencies of the 35delG mutation of the GJB2 gene in different Brazilian regions.

Oliveira CA, Pimpinati CJ, Alexandrino F, Magna LA, Maciel-Guerra AT, Sartorato EL. Oliveira CA, et al. Among authors: alexandrino f. Genet Test. 2007 Spring;11(1):1-3. doi: 10.1089/gte.2006.9994. Genet Test. 2007. PMID: 17394388

8

Molecular findings in Brazilian patients with osteogenesis imperfecta.

Reis FC, Alexandrino F, Steiner CE, Norato DY, Cavalcanti DP, Sartorato EL. Reis FC, et al. Among authors: alexandrino f. J Appl Genet. 2005;46(1):105-8. J Appl Genet. 2005. PMID: 15741671

9

[Prospects for genetic hearing loss screening: 35delG mutation tracking in a newborn population].

Piatto VB, Oliveira CA, Alexandrino F, Pimpinati CJ, Sartorato EL. Piatto VB, et al. Among authors: alexandrino f. J Pediatr (Rio J). 2005 Mar-Apr;81(2):139-42. J Pediatr (Rio J). 2005. PMID: 15858675 Portuguese.

10

Frequency of the 35delG mutation in the GJB2 gene in samples of European, Asian, and African Brazilians.

Oliveira CA, Alexandrino F, Abe-Sandes K, Silva WA Jr, Maciel-Guerra AT, Magna LA, Sartorato EL. Oliveira CA, et al. Among authors: alexandrino f. Hum Biol. 2004 Apr;76(2):313-6. doi: 10.1353/hub.2004.0035. Hum Biol. 2004. PMID: 15359540

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