Table of contents

Letters to JMG

• Spondyloepimetaphyseal dysplasia with multiple dislocations (Hall type): three further cases and evidence of autosomal dominant inheritance (1 September, 2002)

  C M Hall, N H Elcioglu, K D MacDermot, A C Offiah, R M Winter
• Familial chronic nail candidiasis with ICAM-1 deficiency: a new form of chronic mucocutaneous candidiasis (1 September, 2002)

  D Zuccarello, D C Salpietro, S Gangemi, V Toscano, M V Merlino, S Briuglia, G Bisignano, M Mangino, R Mingarelli, B Dallapiccola
• Expression of wild type and mutant TSC2, but not TSC1, causes an increase in the G1 fraction of the cell cycle in HEK293 cells

  (1 September, 2002)

  L Khare, A Astrinidis, W Senapedis, P D Adams, E Petri Henske
• Mutation in KCNQ1 that has both recessive and dominant characteristics

  (1 September, 2002)

  A Murray, F Potet, C Bellocq, I Baró, W Reardon, H E Hughes, S Jeffery
• Heterozygous truncating mutation in the human homeobox gene GSH2 has no discernable phenotypic effect

  (1 September, 2002)

  J G Dauwerse, C E M de Die-Smulders, E Bakker, M H Breuning, D J M Peters
• Coping style, psychological distress, risk perception, and satisfaction in subjects attending genetic counselling for hereditary cancer (1 September, 2002)

  K Nordin, A Lidén, M Hansson, R Rosenquist, G Berglund
• Genetic counselling for familial breast and ovarian cancer in Ontario (1 September, 2002)

  A Andermann, S A Narod
• The use of audiotapes in consultations with women from high risk breast cancer families: a randomised trial (1 September, 2002)

  E Lobb, P Butow, B Meiser, A Barratt, J Kirk, M Gattas, E Haan, K Tucker