Table of contents

Research Article

• Psychosocial genetics: an emerging scientific discipline. (1 July, 1993)

  P S Harper
• What young people think and do when the option for cystic fibrosis carrier testing is available. (1 July, 1993)

  J Mitchell, C R Scriver, C L Clow, F Kaplan
• Prenatal screening for cystic fibrosis: psychological effects on carriers and their partners. (1 July, 1993)

  M E Mennie, M E Compton, A Gilfillan, W A Liston, I Pullen, D A Whyte, D J Brock
• Five year study of prenatal testing for Huntington's disease: demand, attitudes, and psychological assessment. (1 July, 1993)

  S Adam, S Wiggins, P Whyte, M Bloch, M H Shokeir, H Soltan, W Meschino, A Summers, O Suchowersky, J P Welch
• Perception of predictive testing for Huntington's disease by young women: preferring uncertainty to certainty? (1 July, 1993)

  M Decruyenaere, G Evers-Kiebooms, H Van den Berghe
• Genetic risk: women's understanding of carrier risks in Duchenne muscular dystrophy. (1 July, 1993)

  E P Parsons, A J Clarke
• Neurofibromatosis type 1 (NF1): knowledge, experience, and reproductive decisions of affected patients and families. (1 July, 1993)

  C M Benjamin, A Colley, D Donnai, H Kingston, R Harris, L Kerzin-Storrar
• Psychosocial issues raised by a familial ovarian cancer register. (1 July, 1993)

  J Green, F Murton, H Statham
• 'Inside-out', back-to-front: a model for clinical population genetic screening. (1 July, 1993)

  D Shickle, I Harvey
• Childhood onset autosomal dominant polycystic kidney disease in sibs: clinical picture and recurrence risk. German Working Group on Paediatric Nephrology (Arbeitsgemeinschaft für Pädiatrische Nephrologie. (1 July, 1993)

  K Zerres, S Rudnik-Schöneborn, F Deget
• Facioscapulohumeral muscular dystrophy: aspects of genetic counselling, acceptance of preclinical diagnosis, and fitness. (1 July, 1993)

  S Eggers, M R Passos-Bueno, M Zatz
• An epidemiological study of isolated split hand/foot in Hungary, 1975-1984. (1 July, 1993)

  A E Czeizel, M Vitéz, I Kodaj, W Lenz
• Second polar body incorporation into a blastomere results in 46,XX/69,XXX mixoploidy. (1 July, 1993)

  U Müller, J L Weber, P Berry, K G Kupke
• Trisomy 10qter confirmed by in situ hybridisation. (1 July, 1993)

  V Briscioli, G Floridia, E Rossi, A Selicorni, F Lalatta, O Zuffardi
• Deletion of chromosome 2 (p11-p13): case report and review. (1 July, 1993)

  V P Prasher, V H Krishnan, D J Clarke, C T Maliszewska, J A Corbett
• Two sibs with unbalanced translocations in the Waardenburg gene region. (1 July, 1993)

  L I al Gazali, R Quaife
• Mild phenotypic manifestation of a 7p15.3p21.2 deletion. (1 July, 1993)

  C Wang, S Maynard, T W Glover, L G Biesecker
• Extra G positive band on the long arm of chromosome 9. (1 July, 1993)

  L A Knight, G M Soon, M Tan
• Triple structural mosaicism of chromosome 18 in a child with MR/MCA syndrome and abnormal skin pigmentation. (1 July, 1993)

  E Bocian, T Mazurczak, E Buława, H Stańczak, G Rowicka
• Presymptomatic testing for autosomal dominant spinocerebellar ataxia type 1. (1 July, 1993)

  A E Shrimpton, R Davidson, N MacDonald, D J Brock
• Dyskeratosis congenita: three additional families show linkage to a locus in Xq28. (1 July, 1993)

  R Arngrimsson, I Dokal, L Luzzatto, J M Connor
• Cystic fibrosis and deafness. (1 July, 1993)

  J C Llerena Júnior, W Degrave, A De Miranda, P Suffys
• Approaches to prenatal cystic fibrosis carrier screening. (1 July, 1993)

  D Brock
• Severe cystic fibrosis in a child homozygous for the G542 nonsense mutation in the CFTR gene. (1 July, 1993)

  T Bienvenu, C Beldjord, N Fonknechten, J C Kaplan, G Lenoir
• Cutis laxa and the Costello syndrome. (1 July, 1993)

  M A Patton, M Baraitser