Table of contents

Original articles

• Novel deletions of 14q11.2 associated with developmental delay, cognitive impairment and similar minor anomalies in three children (1 June, 2007)

  Farah Zahir, Helen V Firth, Agnes Baross, Allen D Delaney, Patrice Eydoux, William T Gibson, Sylvie Langlois, Howard Martin, Lionel Willatt, Marco A Marra, Jan M Friedman
• The C20orf133 gene is disrupted in a patient with Kabuki syndrome

  (23 June, 2007)

  Nicole M C Maas, Tom Van de Putte, Cindy Melotte, Annick Francis, Constance T R M Schrander-Stumpel, Damien Sanlaville, David Genevieve, Stanislas Lyonnet, Boyan Dimitrov, Koenraad Devriendt, Jean-Pierre Fryns, Joris R Vermeesch
• Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairment

  (18 May, 2007)

  E Van Eyken, G Van Camp, E Fransen, V Topsakal, J J Hendrickx, K Demeester, P Van de Heyning, E Mäki-Torkko, S Hannula, M Sorri, M Jensen, A Parving, M Bille, M Baur, M Pfister, A Bonaconsa, M Mazzoli, E Orzan, A Espeso, D Stephens, K Verbruggen, J Huyghe, I Dhooge, P Huygen, H Kremer, C W R J Cremers, S Kunst, M Manninen, I Pyykkö, A Lacava, M Steffens, T F Wienker, L Van Laer
• Cowden syndrome and Bannayan–Riley–Ruvalcaba syndrome represent one condition with variable expression and age-related penetrance: results of a clinical study of PTEN mutation carriers

  (25 May, 2007)

  K L Lachlan, A M Lucassen, D Bunyan, I K Temple