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Coco M, Salvinelli F, Greco F, et al. Significance of heterozygosis M34T mutation of GJB2 gene in non-syndromic congenital deafness. Retrospective analysis of 12,472 samples of amniotic fluid. J Prenat Med. 2013;7(4):56-8
Coco, M., Salvinelli, F., Greco, F., Trivelli, M., D'Emidio, L., Mesoraca, A., Giorlandino, C., Raffio, R., & Coco, C. (2013). Significance of heterozygosis M34T mutation of GJB2 gene in non-syndromic congenital deafness. Retrospective analysis of 12,472 samples of amniotic fluid. Journal of prenatal medicine, 7(4), 56-8.
Coco, Manuela, et al. "Significance of heterozygosis M34T mutation of GJB2 gene in non-syndromic congenital deafness. Retrospective analysis of 12,472 samples of amniotic fluid." Journal of prenatal medicine vol. 7,4 (2013): 56-8.
Coco M, Salvinelli F, Greco F, Trivelli M, D'Emidio L, Mesoraca A, Giorlandino C, Raffio R, Coco C. Significance of heterozygosis M34T mutation of GJB2 gene in non-syndromic congenital deafness. Retrospective analysis of 12,472 samples of amniotic fluid. J Prenat Med. 2013 Oct;7(4):56-8. PMID: 24611097; PMCID: PMC3931280.
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