Table of contents

Letters to the editor

• Dutch patients with glycogen storage disease type II show common ancestry for the 525delT and del exon 18 mutations (1 August, 2001)

  Margreet G E M Ausems, Klara ten Berg, Lodewijk A Sandkuijl, Marian A Kroos, Alfons F J Bardoel, Katerina N Roumelioti, Arnold J J Reuser, Richard Sinke, Cisca Wijmenga
• Recurrent mutations in the deafness geneGJB2 (connexin 26) in British Asian families

  (1 August, 2001)

  Sarah Rickard, David P Kelsell, Tony Sirimana, Kaukab Rajput, Breege MacArdle, Maria Bitner-Glindzicz
• A region of homozygosity within 22q11.2 associated with congenital heart disease: recessive DiGeorge/velocardiofacial syndrome? (1 August, 2001)

  Judy Henwood, Chris Pickard, Jack P Leek, Christopher P Bennett, Yanick J Crow, John D R Thompson, Mushtaq Ahmed, Kevin G Watterson, Jonathan M Parsons, Emma Roberts, Nicholas J Lench
• High frequency of the ApoB-100 R3500Q mutation in Bulgarian hypercholesterolaemic subjects

  (1 August, 2001)

  Anelia Horvath, Alexey Savov, Stephen Kirov, Elina Karshelova, Iva Paskaleva, Assen Goudev, Varban Ganev
• A community based study on intentions regarding predictive testing for hereditary breast cancer (1 August, 2001)

  M Welkenhuysen, G Evers-Kiebooms, M Decruyenaere, E Claes, L Denayer
• Ocular malformations, postaxial polydactyly, and delayed intramembranous ossification: a new autosomal dominant condition (1 August, 2001)

  Donna M Martin, Jerome L Gorski
• Recessively inherited lower incisor hypodontia (1 August, 2001)

  Sinikka Pirinen, Anu Kentala, Pekka Nieminen, Teppo Varilo, Irma Thesleff, Sirpa Arte
• Congenital diaphragmatic hernia and interstitial deletion of chromosome 3 (1 August, 2001)

  P Brennan, G D Croaker, M Heath
• A supernumerary marker chromosome with a neocentromere derived from 5p14→pter (1 August, 2001)

  Barbara Fritz, Ilona Dietze, Annelise Wandall, Mücehver Aslan, Angela Schmidt, Evelyn Kattner, Robin Schwerdtfeger, Ursula Friedrich
• A case of Roberts syndrome described in 1737 (1 August, 2001)

  A W Bates