Coco, M., Salvinelli, F., Greco, F., Trivelli, M., D'Emidio, L., Mesoraca, A., . . . 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.
Style de citation ChicagoCoco, Manuela, Fabrizio Salvinelli, Fabio Greco, Maurizio Trivelli, Laura D'Emidio, Alvaro Mesoraca, Claudio Giorlandino, Raffaella Raffio, et Claudio Coco. "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, no. 4 (2013): 56.
Style de citation MLACoco, 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, no. 4, 2013, p. 56.