Table of contents

Letters to JMG

• 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

  (1 July, 2005)

  F J del Castillo, M Rodríguez-Ballesteros, A Álvarez, T Hutchin, E Leonardi, C A de Oliveira, H Azaiez, Z Brownstein, M R Avenarius, S Marlin, A Pandya, H Shahin, K R Siemering, D Weil, W Wuyts, L A Aguirre, Y Martín, M A Moreno-Pelayo, M Villamar, K B Avraham, H-H M Dahl, M Kanaan, W E Nance, C Petit, R J H Smith, G Van Camp, E L Sartorato, A Murgia, F Moreno, I del Castillo
• A genome screen of families at high risk for Hodgkin lymphoma: evidence for a susceptibility gene on chromosome 4 (1 July, 2005)

  L R Goldin, M L McMaster, M Ter-Minassian, S Saddlemire, B Harmsen, G Lalonde, M A Tucker
• Breast and ovarian cancer risks to carriers of the BRCA1 5382insC and 185delAG and BRCA2 6174delT mutations: a combined analysis of 22 population based studies (1 July, 2005) Free

  A C Antoniou, P D P Pharoah, S Narod, H A Risch, J E Eyfjord, J L Hopper, H Olsson, O Johannsson, Å Borg, B Pasini, P Radice, S Manoukian, D M Eccles, N Tang, E Olah, H Anton-Culver, E Warner, J Lubinski, J Gronwald, B Gorski, H Tulinius, S Thorlacius, H Eerola, H Nevanlinna, K Syrjäkoski, O-P Kallioniemi, D Thompson, C Evans, J Peto, F Lalloo, D G Evans, D F Easton
• Association of two tumour necrosis factor gene polymorphisms with the incidence of severe intraventricular haemorrhage in preterm infants (1 July, 2005)

  A Heep, A C Schueller, E Kattner, M Kroll, J Sander, M Wisbauer, P Bartmann, F Stueber