Table of contents

Research Article

• Splotch locus mouse mutants: models for neural tube defects and Waardenburg syndrome type I in humans. (1 March, 1992)

  C E Moase, D G Trasler
• Family history of breast cancer: how important is it? (1 March, 1992)

  D T Bishop
• Family history and risk of breast cancer. (1 March, 1992)

  R S Houlston, E McCarter, S Parbhoo, J H Scurr, J Slack
• Epidemiology of breast cancer in families in Iceland. (1 March, 1992)

  H Tulinius, H Sigvaldason, G Olafsdóttir, L Tryggvadóttir
• Prenatal prediction of spinal muscular atrophy. (1 March, 1992)

  R J Daniels, G K Suthers, K E Morrison, N H Thomas, M J Francis, C G Mathew, S Loughlin, A Heiberg, D Wood, V Dubowitz
• Prenatal prediction of Werdnig-Hoffmann disease using linked polymorphic DNA probes. (1 March, 1992)

  J Melki, S Abdelhak, P Burlet, V Raclin, J Kaplan, R Spiegel, S Gilgenkrantz, N Philip, M L Chauvet, Y Dumez
• An intrachromosomal insertion causing 5q22 deletion and familial adenomatous polyposis coli in two generations. (1 March, 1992)

  I Cross, J Delhanty, P Chapman, L V Bowles, D Griffin, J Wolstenholme, M Bradburn, J Brown, C Wood, A Gunn
• Prenatal diagnosis and presymptomatic detection of neurofibromatosis type 1. (1 March, 1992)

  M Upadhyaya, A Fryer, J MacMillan, W Broadhead, S M Huson, P S Harper
• Clinical variability of type 1 neurofibromatosis: is there a neurofibromatosis-Noonan syndrome? (1 March, 1992)

  H J Stern, H M Saal, J S Lee, P R Fain, D E Goldgar, K N Rosenbaum, D F Barker
• Absence of linkage of Noonan syndrome to the neurofibromatosis type 1 locus. (1 March, 1992)

  M Sharland, R Taylor, M A Patton, S Jeffery
• Analysis of quantitative PCR for the diagnosis of deletion and duplication carriers in the dystrophin gene. (1 March, 1992)

  S Abbs, M Bobrow
• Distal spinal muscular atrophy with vocal cord paralysis. (1 March, 1992)

  C Pridmore, M Baraitser, E M Brett, A E Harding
• Unusual occurrence of cervical myelopathy in a case of Stickler's syndrome. (1 March, 1992)

  S Noël, D Balériaux, N Telerman-Toppet
• A new form of infantile spinal muscular atrophy. (1 March, 1992)

  A García-Alix, J I Rodriguez, J Quero
• MASA syndrome (a form of complicated spastic paraplegia) and X linked hydrocephalus: variable expression of the same mutation at Xq28? Call for families. (1 March, 1992)

  C Schrander-Stumpel, J Fryns, J J Cassiman, E Legius, A Spaepen, C J Höweler