Table of contents

Research Article

• The genetic testing of children. (1 October, 1994)

  T M Marteau
• Genetic linkage to the type VII collagen gene (COL7A1) in 26 families with generalised recessive dystrophic epidermolysis bullosa and anchoring fibril abnormalities. (1 October, 1994)

  M G Dunnill, A J Richards, G Milana, F Mollica, D Atherton, I Winship, M Farrall, L al-Imara, R A Eady, F M Pope
• Mosaic uniparental disomy in Beckwith-Wiedemann syndrome. (1 October, 1994)

  R E Slatter, M Elliott, K Welham, M Carrera, P N Schofield, D E Barton, E R Maher
• X inactivation patterns in female monozygotic twins and their families. (1 October, 1994)

  E Watkiss, T Webb, G Rysiecki, N Girdler, E Hewett, S Bundey
• Cephalometric analysis of Rapp-Hodgkin syndrome. (1 October, 1994)

  T C Hart, S Kyrkanides
• Phenotypic variation of tuberous sclerosis in a single extended kindred. (1 October, 1994)

  S L Smalley, F Burger, M Smith
• Absence of linkage between idiopathic dilated cardiomyopathy and candidate genes involved in the immune function in a large Italian pedigree. (1 October, 1994)

  M Krajinovic, L Mestroni, G M Severini, B Pinamonti, F Camerini, A Falaschi, M Giacca
• Osteocraniostenosis. (1 October, 1994)

  A Verloes, F Narcy, B Grattagliano, A L Delezoide, P Guibaud, J P Schaaps, M Le Merrer, P Maroteaux
• Albright's hereditary osteodystrophy. (1 October, 1994)

  L C Wilson, R C Trembath
• The genetic testing of children. Working Party of the Clinical Genetics Society (UK) (1 October, 1994)

  A Clarke
• Intrachromosomal triplication of 15q11-q13. (1 October, 1994)

  A A Schinzel, L Brecevic, F Bernasconi, F Binkert, F Berthet, A Wuilloud, W P Robinson
• A newborn with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. (1 October, 1994)

  G Calabrese, P G Franchi, L Stuppia, R Mingarelli, C Rossi, L Ramenghi, M Marino, E Morizio, R Peila, A Antonucci
• Down-Turner syndrome: case report and review. (1 October, 1994)

  G J Van Buggenhout, B C Hamel, J C Trommelen, H Mieloo, D F Smeets
• Linkage and mutation analysis in an extended family with Charcot-Marie-Tooth disease type 1B. (1 October, 1994)

  E Nelis, V Timmerman, P De Jonghe, L Muylle, J J Martin, C Van Broeckhoven
• Chimaerism shown by cytogenetics and DNA polymorphism analysis. (1 October, 1994)

  A J Green, D E Barton, P Jenks, J Pearson, J R Yates
• Huntington's disease in two unrelated Arab kindreds and in an Afghani family resident in Saudi Arabia. (1 October, 1994)

  E M Scrimgeour, S A Tahoon, T H Zawawi
• The Prader-Willi-like phenotype in fragile X patients: a designation facilitating clinical (and molecular) differential diagnosis. (1 October, 1994)

  B B De Vries, M F Niermeijer
• Arthrogryposis multiplex congenita, renal dysfunction, and cholestasis syndrome. (1 October, 1994)

  J M Saraiva, H C Mota