Table of contents

Research Article

• Cone and cone-rod dystrophies. (1 May, 1992)

  A T Moore
• X linked progressive cone dystrophy with specific attention to carrier detection. (1 May, 1992)

  J A van Everdingen, L N Went, J E Keunen, J A Oosterhuis
• Late onset dominant cone dystrophy with early blue cone involvement. (1 May, 1992)

  L N Went, M J van Schooneveld, J A Oosterhuis
• Reverse chromosome painting: a method for the rapid analysis of aberrant chromosomes in clinical cytogenetics. (1 May, 1992)

  N P Carter, M A Ferguson-Smith, M T Perryman, H Telenius, A H Pelmear, M A Leversha, M T Glancy, S L Wood, K Cook, H M Dyson
• Prenatal cystic fibrosis carrier testing: designing an information leaflet to meet the specific needs of the target population. (1 May, 1992)

  M E Mennie, W A Liston, D J Brock
• Principles and practicalities of carrier screening: attitudes of recent parents. (1 May, 1992)

  J M Green
• Familial screening for genetic haemochromatosis by means of DNA markers. (1 May, 1992)

  J Yaouanq, A el Kahloun, M Chorney, A M Jouanolle, V Mauvieux, M Perichon, M Blayau, P Pontarotti, J Y Le Gall, V David
• Ectodermal dysplasia with blindness in sibs on the island of Rodrigues. (1 May, 1992)

  C E Wallis, P Beighton
• Oculoauriculovertebral spectrum and cerebral anomalies. (1 May, 1992)

  C T Schrander-Stumpel, C E de Die-Smulders, R C Hennekam, J P Fryns, P X Bouckaert, O F Brouwer, J J da Costa, E J Lommen, P D Maaswinkel-Mooy
• Weaver syndrome. (1 May, 1992)

  T R Cole, N R Dennis, H E Hughes
• Small cell lung carcinoma in a patient with Sotos syndrome: are genes at 3p21 involved in both conditions? (1 May, 1992)

  T R Cole, H E Hughes, M J Jeffreys, G T Williams, M M Arnold
• Monosomy 10qter: a new case. (1 May, 1992)

  M Teyssier, C Charrin, J Dutruge, C Rousselle
• Tandem duplication of the terminal band of the long arm of chromosome 7 (dir dup (7)(q36----qter)). (1 May, 1992)

  R S Verma, R A Conte, J H Pitter
• Brachydactyly type C associated with shortening of the hallux. (1 May, 1992)

  J M Rowe-Jones, A L Moss, M A Patton
• Atypical case of Aarskog syndrome. (1 May, 1992)

  R V Mikelsaar, I W Lurie
• A de novo insertion, detected prenatally, with normal phenotype. (1 May, 1992)

  A F Hashish, N A Monk, A J Watt, R J Gardner
• The molecular genetics of Alport syndrome: report of two workshops. (1 May, 1992)

  F Flinter, M Bobrow
• Symposium on epidermolysis bullosa. (1 May, 1992)

  T Gedde-Dahl
• X linked alpha thalassaemia/mental retardation (ATR-X) syndrome. (1 May, 1992)

  A E Chudley, R B Lowry
• 49,XXXXY syndrome: behavioural and developmental profiles. (1 May, 1992)

  J Jancar