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