Table of contents

Letters to JMG

• Disruption of an exon splicing enhancer in exon 3 of MLH1 is the cause of HNPCC in a Quebec family

  (27 May, 2005)

  S McVety, L Li, P H Gordon, G Chong, W D Foulkes
• Espin gene (ESPN) mutations associated with autosomal dominant hearing loss cause defects in microvillar elongation or organisation

  (1 June, 2005)

  F Donaudy, L Zheng, R Ficarella, E Ballana, M Carella, S Melchionda, X Estivill, J R Bartles, P Gasparini
• Congenital heart defects and genetic variants in the methylenetetrahydroflate reductase gene (10 June, 2005)

  C A Hobbs, S J James, A Parsian, P A Krakowiak, S Jernigan, J J Greenhaw, Y Lu, M A Cleves
• The Pro279Leu variant in the transcription factor MEF2A is associated with myocardial infarction (15 June, 2005)

  P González, M García-Castro, J R Reguero, A Batalla, A G Ordóñez, R L Palop, I Lozano, M Montes, V Álvarez, E Coto
• A novel locus for autosomal dominant non-syndromic deafness, DFNA53, maps to chromosome 14q11.2-q12 (15 June, 2005)

  D Yan, X Ke, S H Blanton, X M Ouyang, A Pandya, L L Du, W E Nance, X Z Liu
• Sequence variation in mitochondrial complex I genes: mutation or polymorphism? (21 June, 2005)

  A L Mitchell, J L Elson, N Howell, R W Taylor, D M Turnbull
• Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents (24 June, 2005)

  C Rosenberg, J Knijnenburg, E Bakker, A M Vianna-Morgante, W Sloos, P A Otto, M Kriek, K Hansson, A C V Krepischi-Santos, H Fiegler, N P Carter, E K Bijlsma, A van Haeringen, K Szuhai, H J Tanke
• Androgenetic/biparental mosaicism causes placental mesenchymal dysplasia (20 May, 2005)

  K A Kaiser-Rogers, D E McFadden, C A Livasy, J Dansereau, R Jiang, J F Knops, L Lefebvre, K W Rao, W P Robinson