RT Journal Article SR Electronic T1 A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment JF Journal of Medical Genetics JO J Med Genet FD BMJ Publishing Group Ltd SP 588 OP 594 DO 10.1136/jmg.2004.028324 VO 42 IS 7 A1 del Castillo, F J A1 Rodríguez-Ballesteros, M A1 Álvarez, A A1 Hutchin, T A1 Leonardi, E A1 de Oliveira, C A A1 Azaiez, H A1 Brownstein, Z A1 Avenarius, M R A1 Marlin, S A1 Pandya, A A1 Shahin, H A1 Siemering, K R A1 Weil, D A1 Wuyts, W A1 Aguirre, L A A1 Martín, Y A1 Moreno-Pelayo, M A A1 Villamar, M A1 Avraham, K B A1 Dahl, H-H M A1 Kanaan, M A1 Nance, W E A1 Petit, C A1 Smith, R J H A1 Van Camp, G A1 Sartorato, E L A1 Murgia, A A1 Moreno, F A1 del Castillo, I YR 2005 UL http://jmg.bmj.com/content/42/7/588.abstract AB