Table of contents

Letters to JMG

• Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis

  (17 October, 2008)

  H Daoud, P N Valdmanis, E Kabashi, P Dion, N Dupré, W Camu, V Meininger, G A Rouleau
• Investigation of somatic NKX2-5 mutations in congenital heart disease

  (30 January, 2009)

  J M Draus, M A Hauck, M Goetsch, E H Austin, A Tomita-Mitchell, M E Mitchell
• Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practice (17 November, 2008)

  D L Bruno, D Ganesamoorthy, J Schoumans, A Bankier, D Coman, M Delatycki, R J M Gardner, M Hunter, P A James, P Kannu, G McGillivray, N Pachter, H Peters, C Rieubland, R Savarirayan, I E Scheffer, L Sheffield, T Tan, S M White, A Yeung, Z Bowman, C Ngo, K W Choy, V Cacheux, L Wong, D J Amor, H R Slater
• Effect of CHEK2 missense variant I157T on the risk of breast cancer in carriers of other CHEK2 or BRCA1 mutations

  (17 October, 2008)

  C Cybulski, B Górski, T Huzarski, T Byrski, J Gronwald, T Dębniak, D Wokołorczyk, A Jakubowska, P Serrano-Fernández, T Dork, S A Narod, J Lubiński