Table of contents

Original articles

• General overgrowth in the fragile X syndrome: variability in the phenotypic expression of the FMR1 gene mutation (1 October, 1995)

  Bert B A de Vries, Hazel Robinson, Irene Stolte-Dijkstra, Cecil V Tjon Pian Gi, Piet F Dijkstra, Jaap van Doorn, Dicky J J Halley, Ben A Oostra, Gillian Turner, Martinus F Niermeijer
• Exclusion mapping of chromosomal regions which cross hybridise to FSHD1A associated markers in FSHD1B (1 October, 1995)

  J R Gilbert, M C Speer, J Stajich, R Clancy, K Lewis, H Qiu, L Yamaoka, A Kumar, J Vance, C Stewart, M Rozear, A D Roses, M A Pericak-Vance
• Linkage analysis in blepharophimosis-ptosis syndrome confirms localisation to 3q21-24 (1 October, 1995)

  H S Harrar, S Jeffery, M A Patton
• Bilateral cataract and high serum ferritin: a new dominant genetic disorder? (1 October, 1995)

  Dominique Bonneau, Isabelle Winter-Fuseau, Marie-Noëlle Loiseau, Patrizia Amati, Michel Berthier, Denis Oriot, Carole Beaumont
• Current issues of personnel and laboratory practices in genetic testing (1 October, 1995)

  Hon Fong Louie Mark, Thaddeus Kelly, Michael S Watson, Gerald Hoeltge, Wayne A Miller, Laurent Beauregard
• Metachromatic leucodystrophy (MLD) in a patient with a constitutional ring chromosome 22 (1 October, 1995)

  M B Coulter-Mackie, J Rip, M D Ludman, J Beis, D E C Cole
• Familial partial trisomy 8p without dysmorphic features and only mild mental retardation (1 October, 1995)

  J J M Engelen, C E M de Die-Smulders, J M J Sijstermans, L E C Meers, J C M Albrechts, A J H Hamers
• Public attitudes towards the selection of desirable characteristics in children (1 October, 1995)

  Theresa Marteau, Susan Michie, Harriet Drake, Martin Bobrow
• Adolescents' opinions about genetic risk information, prenatal diagnosis, and pregnancy termination (1 October, 1995)

  Marleen Decruyenaere, Gerry Evers-Kiebooms, Myriam Welkenhuysen, Jacqueline Bande-Knops, Veerle Van Gerven, Herman Van den Berghe