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Lack of association between optineurin gene variants T34T, E50K, M98K, 691_692insAG and R545Q and primary open angle glaucoma in Brazilian patients.
Caixeta-Umbelino C, de Vasconcellos JP, Costa VP, Kasahara N, Della Paolera M, de Almeida GV, Cohen R, Mandia C Jr, Rocha MN, Richeti F, Longui CA, de Melo MB. Caixeta-Umbelino C, et al. Among authors: longui ca. Ophthalmic Genet. 2009 Mar;30(1):13-8. doi: 10.1080/13816810802502970. Ophthalmic Genet. 2009. PMID: 19172505
Molecular detection of XO - Turner syndrome.
Longui CA, Rocha MN, Martinho LC, Gomes GG, de Miranda RE, Lima TA, Melo MB, Monte O. Longui CA, et al. Genet Mol Res. 2002 Sep 30;1(3):266-70. Genet Mol Res. 2002. PMID: 14963834 Free article.
Inhibin alpha-subunit (INHA) gene and locus changes in paediatric adrenocortical tumours from TP53 R337H mutation heterozygote carriers.
Longui CA, Lemos-Marini SH, Figueiredo B, Mendonca BB, Castro M, Liberatore R Jr, Watanabe C, Lancellotti CL, Rocha MN, Melo MB, Monte O, Calliari LE, Guerra-Junior G, Baptista MT, Sbragia-Neto L, Latronico AC, Moreira A, Tardelli AM, Nigri A, Taymans SE, Stratakis CA. Longui CA, et al. J Med Genet. 2004 May;41(5):354-9. doi: 10.1136/jmg.2004.018978. J Med Genet. 2004. PMID: 15121773 Free PMC article.
108 results