Table of contents

Research Article

• An exclusion map for facioscapulohumeral (Landouzy-Déjérine) disease. (1 August, 1989) Free

  M Sarfarazi, M Upadhyaya, G Padberg, M Pericak-Vance, T Siddique, G Lucotte, P Lunt
• Linkage analysis of French families with facioscapulohumeral muscular dystrophy. (1 August, 1989) Free

  G Lucotte, S Berriche, M Fardeau
• Linkage analysis in the spinal muscular atrophy type of facioscapulohumeral disease. (1 August, 1989) Free

  T Siddique, H Roper, M A Pericak-Vance, J Shaw, K L Warner, W Y Hung, K L Phillips, P Lunt, W J Cumming, A D Roses
• A genetic linkage study of facioscapulohumeral (Landouzy-Déjérine) disease with 24 polymorphic DNA probes. (1 August, 1989) Free

  M Upadhyaya, M Sarfarazi, P W Lunt, W Broadhead, P S Harper
• A study of familial hypercholesterolaemia in Iceland using RFLPs. (1 August, 1989) Free

  R Taylor, J Bryant, V Gudnason, G Sigurdsson, S Humphries
• Identification of the haplotype pattern associated with the mutant PKU allele in the Gypsy population of Wales. (1 August, 1989) Free

  L A Tyfield, A L Meredith, M J Osborn, P S Harper
• Cone-rod congenital amaurosis associated with congenital hypertrichosis: an autosomal recessive condition. (1 August, 1989) Free

  I K Jalili
• Evidence for genetic heterogeneity in tuberous sclerosis. (1 August, 1989) Free

  J R Sampson, J R Yates, L A Pirrit, P Fleury, I Winship, P Beighton, J M Connor
• Pitfalls in counselling of the blepharophimosis, ptosis, epicanthus inversus syndrome (BPES) (1 August, 1989) Free

  I K Temple, M Baraitser
• Hypohidrotic ectodermal dysplasia, primary hypothyroidism, and agenesis of the corpus callosum. (1 August, 1989) Free

  J P Fryns, K Chrzanowska, H Van den Berghe
• Auralcephalosyndactyly: a new craniosynostosis syndrome or a variant of the Saethre-Chotzen syndrome? (1 August, 1989) Free

  E Legius, J P Fryns, H Van den Berghe
• Familial translocation t(9;16). (1 August, 1989) Free

  C Dowman, D Lockwood, J Allanson
• De novo terminal deletion 7p22.1--pter in a child without craniosynostosis. (1 August, 1989) Free

  F Speleman, M Craen, J Leroy
• A non-centromeric C band variant on chromosome 11q23.2. (1 August, 1989) Free

  D K Spak, K Johnston, T A Donlon
• A workshop on facioscapulohumeral (Landouzy-Déjérine) disease, Manchester, 16 to 17 November 1988. (1 August, 1989) Free

  P W Lunt
• Angelman's syndrome and 15q11-13 deletions. (1 August, 1989) Free

  J P Fryns, A Kleczkowska, P Decock, H Van den Berghe
• Anencephaly: a vanishing problem in Bedouins? (1 August, 1989) Free

  T I Farag, S A al-Awadi, S Yassin, T A el-Kassaby, S Jaefary, R Usha, R Uma, S A Mady, M Fakhr, M Mannae
• Autosomal dominant sneezing disorder provoked by fullness of stomach. (1 August, 1989) Free

  A S Teebi, Q A al-Saleh