Table of contents

Research Article

• Screening for fetal and genetic abnormality: social and ethical issues. (1 May, 1988)

  R Harris
• Screening for fetal and genetic abnormality: social and ethical issues. (1 May, 1988)

  G R Dunstan
• Genetic markers on chromosome 7. (1 May, 1988)

  L C Tsui
• Meiotic recombination in the beta globin gene cluster causing an error in prenatal diagnosis of beta thalassaemia. (1 May, 1988)

  C Camaschella, A Serra, G Saglio, M T Bertero, U Mazza, S Terzoli, B Brambati, L Cremonesi, M Travi, M Ferrari
• Exclusion of calcitonin as a candidate gene for the basic defect in a family with autosomal dominant supravalvular aortic stenosis. (1 May, 1988)

  C P Bennett, J Burn, G E Moore, J Chambers, R Williamson, J Wilkinson
• Sorsby syndrome: a report on further generations of the original family. (1 May, 1988)

  E M Thompson, M Baraitser
• Intrafamilial clinical variability of type 1 Gaucher disease in a French-Canadian family. (1 May, 1988)

  F Y Choy
• Are double translocations double trouble? (1 May, 1988)

  S M Bowser-Riley, M J Griffiths, M R Creasy, P A Farndon, K E Martin, D A Thomson, S A Larkins, R A Johnson, J L Watt
• The acrocallosal syndrome in first cousins: widening of the spectrum of clinical features and further support for autosomal recessive inheritance. (1 May, 1988)

  A Schinzel
• Non-opposable triphalangeal thumb in an Italian family. (1 May, 1988)

  A Warm, C Di Pietro, F D'Agrosa, M Cambiè, F Gaboardi
• Complete absence of external genitalia in limb-body wall complex: two cases. (1 May, 1988)

  A Litwin, P Merlob, M Grunebaum
• The Coffin-Lowry syndrome. (1 May, 1988)

  I D Young
• A lethal short rib syndrome without polydactyly. (1 May, 1988)

  R M Winter
• Intrauterine death in megacystis-microcolon-intestinal hypoperistalsis syndrome. (1 May, 1988)

  S A Farrell
• Lethal osteogenesis imperfecta associated with 46,XY,inv(7)(p13q22) karyotype. (1 May, 1988)

  A S Knisely, A Richardson, D Abuelo, S Casey, D B Singer
• Absence of a vagina and right sided adnexa uteri in the Waardenburg syndrome: a possible clue to the embryological defect. (1 May, 1988)

  R M Goodman, G Oelsner, M Berkenstadt, D Admon
• Trisomy 3 mosaicism in a patient with Bartter syndrome. (1 May, 1988)

  F De Keyser, E Matthys, A De Paepe, M R Verschraegen-Spae, M Matton