Table of contents

Research Article

• A newly defined X linked mental retardation syndrome associated with alpha thalassaemia. (1 November, 1991)

  R J Gibbons, A O Wilkie, D J Weatherall, D R Higgs
• Alpha thalassaemia/mental retardation syndrome (non-deletional type): report of a family supporting X linked inheritance. (1 November, 1991)

  T R Cole, A May, H E Hughes
• X linked alpha thalassaemia/mental retardation: spectrum of clinical features in three related males. (1 November, 1991)

  A O Wilkie, R J Gibbons, D R Higgs, M E Pembrey
• The non-deletion alpha thalassaemia/mental retardation syndrome: further support for X linkage. (1 November, 1991)

  D Donnai, J Clayton-Smith, R J Gibbons, D R Higgs
• A genetic study of neurofibromatosis 1 in south-western Ontario. I. Population, familial segregation of phenotype, and molecular linkage. (1 November, 1991)

  D I Rodenhiser, M B Coulter-Mackie, J H Jung, S M Singh
• Watson syndrome: is it a subtype of type 1 neurofibromatosis? (1 November, 1991)

  J E Allanson, M Upadhyaya, G H Watson, M Partington, A MacKenzie, D Lahey, H MacLeod, M Sarfarazi, W Broadhead, P S Harper
• Substitution of cysteine for glycine at residue 415 of one allele of the alpha 1(I) chain of type I procollagen in type III/IV osteogenesis imperfecta. (1 November, 1991)

  A C Nicholls, J Oliver, D V Renouf, M Keston, F M Pope
• Analysis of mitochondrial DNA in Leber's hereditary optic neuropathy. (1 November, 1991)

  J Poulton, M E Deadman, J Bronte-Stewart, W S Foulds, R M Gardiner
• Mutation and linkage disequilibrium analysis in genetic counselling of Spanish cystic fibrosis families. (1 November, 1991)

  T Casals, V Nunes, C Lázaro, F J Giménez, E Girbau, V Volpini, X Estivill
• Lymphocyte mRNA as a resource for detection of mutations and polymorphisms in the CF gene. (1 November, 1991)

  G Chalkley, A Harris
• Transmission of Proteus syndrome from father to son? (1 November, 1991)

  J Goodship, A Redfearn, D Milligan, D Gardner-Medwin, J Burn
• Microtia and short stature: a new syndrome. (1 November, 1991)

  B Cohen, I K Temple, J C Symons, C M Hall, D G Shaw, M Bhamra, A M Jackson, M E Pembrey
• Ectopia lentis et pupillae: the genetic aspects and differential diagnosis. (1 November, 1991)

  A Colley, I C Lloyd, A Ridgway, D Donnai
• Microcephalic osteodysplastic primordial dwarfism type I/III in sibs. (1 November, 1991)

  P Meinecke, E Passarge
• Three cases of 16q duplication. (1 November, 1991)

  E R Maher, L Willatt, G Cuthbert, C Chapman, S V Hodgson
• Severe manifestations of oculoauriculovertebral spectrum in a cocaine exposed infant. (1 November, 1991)

  M Lessick, R Vasa, J Israel
• Kuwait type faciodigitogenital syndrome. (1 November, 1991)

  A S Teebi, S A al Awadi
• Pericentromeric heterochromatin of chromosome 3. (1 November, 1991)

  S Luke, R S Verma
• Cystic fibrosis in Bulgaria. (1 November, 1991)

  L Kalaydjieva, D Angelicheva, I Galeva, V Lalov, D Konstantinova
• Floating Harbor and the good ship Shprintzen. (1 November, 1991)

  A Lipson