Table of contents

Letters to the editor

• Fine molecular mapping of the 4p16.3 aneuploidy syndromes in four translocation families (1 June, 2000)

  K FAGAN, V SOUBJAKI, P DONALD, G TURNER, M PARTINGTON
• Investigation of meiotic rearrangements in DGS/VCFS patients with a microdeletion 22q11.2 (1 June, 2000)

  DETLEF TROST, WALTER WIEBE, SIEGFRIED UHLHAAS, PETER SCHWINDT, GESA SCHWANITZ
• Pure trisomy 20p resulting from isochromosome formation and whole arm translocation (1 June, 2000)

  R U SIDWELL, M-P PINSON, B GIBBONS, S-A BYATT, E C SVENNEVIK, R J HASTINGS, D M FLYNN
• ASALL1 mutation causes a branchio-oto-renal syndrome-like phenotype

  (1 June, 2000)

  SASKIA ENGELS, JÜRGEN KOHLHASE, JULIE MCGAUGHRAN
• New MR/MCA syndrome with distinct facial appearance and general habitus, broad and webbed neck, hypoplastic inverted nipples, epilepsy, and pachygyria of the frontal lobes (1 June, 2000)

  J-P FRYNS, S AFTIMOS
• The mitochondrial genome in Wolfram syndrome (1 June, 2000)

  TIMOTHY G BARRETT, MARTIN SCOTT-BROWN, ANNEKE SELLER, AMY BEDNARZ, KELVIN POULTON, JOANNA POULTON
• Two further cases of Sener syndrome: frontonasal dysplasia and dilated Virchow-Robin spaces (1 June, 2000)

  S A LYNCH, K HALL, S PRECIOUS, A O M WILKIE, J A HURST
• The psychological impact of a cancer family history questionnaire completed in general practice (1 June, 2000)

  VIRGINIA LEGGATT, JAMES MACKAY, THERESA M MARTEAU, JOHN R W YATES
• Attitudes to genetic testing for breast cancer susceptibility in women at increased risk of developing hereditary breast cancer (1 June, 2000)

  BETTINA MEISER, PHYLLIS BUTOW, ALEXANDRA BARRATT, GRAEME SUTHERS, MERYL SMITH, ALISON COLLEY, ELIZABETH THOMPSON, KATHERINE TUCKER
• Attitudes of von Hippel-Lindau disease patients towards presymptomatic genetic diagnosis in children and prenatal diagnosis (1 June, 2000)

  MICHELINE LEVY, STÉPHANE RICHARD