Table of contents

Research Article

• Oesophageal atresia in the South West of England. (1 March, 1975)

  T J David, S E O'Callaghan
• A genetic study of torsion dystonia. (1 March, 1975)

  S Bundey, M J Harrison, C D Marsden
• Clinical and ultrastructural observations in a kindred with normo-hyperkalaemic periodic paralysis. (1 March, 1975)

  T S Danowski, E R Fisher, C Vidalon, J W Vester, R Thompson, S Nolan, T Stephan, J H Sunder
• Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring. (1 March, 1975)

  R H Lindenbaum, M Bobrow
• Giemsa banding of chromosome 1gh+ and linkage analysis. (1 March, 1975)

  P N Howard, G R Stoddard, M W Goddard, J R Seely
• Distinction between Duchenne and other muscular dystrophies by ribosomal protein synthesis. (1 March, 1975)

  V Ionasescu
• Thalassaemia in northern Liberia. A survey in the Mount Nimba area. (1 March, 1975)

  M C Willcox
• Estimation of the age at onset of Huntington's disease from factors associated with the affected parent. (1 March, 1975)

  C J Brackenridge, B Teltscher
• The occurrence of gonadal dysgenesis in association with monozygotic twinning. (1 March, 1975)

  L Karp, J I Bryant, G Tagatz, E Giblett, P J Fialkow
• A family study of coeliac disease. (1 March, 1975)

  T J David, A B Ajdukiewicz
• Haemoglobin Lepore Boston and elliptocytosis in a family of Indonesian-German ancestry. (1 March, 1975)

  L N Went, W W de Jong, S E Bos
• Aglossia-adactylia syndrome. (1 March, 1975)

  N C Nevin, D Burrows, G Allen, D C Kernohan
• A family with apparently sex-linked optic atrophy. (1 March, 1975)

  L N Went, E C De Vries-De Mol, H J Völker-Dieben
• Deletion of the short arm of chromosome No. 10. (1 March, 1975)

  M H Shokeir, M Ray, J L Hamerton, F Bauder, H O'Brien
• Trisomy 13 and Rubinstein-Taybi syndrome. (1 March, 1975)

  F P Garcia, L Y Hsu, H Fox, D Gribetz
• Partial 12p deletion: a cause for a mental retardation, multiple congenital abnormality syndrome. (1 March, 1975)

  N C Magnelli, E Therman
• Prenatal diagnosis of a neural tube defect: Meckel syndrome. (1 March, 1975)

  M J Seller
• A case of hyalinosis cutis et mucosae (lipoid proteinosis of Urbach and Wiethe) with common ancestors in four remote generations. (1 March, 1975)

  R C Juberg, P R Winder, L L Turk
• Neonatal testicular torsion in two brothers. (1 March, 1975)

  E E Castilla, R Sod, O Anzorena, J Texido
• Letter: Klinefelter's syndrome and maternal XX/XXX mosaicism. (1 March, 1975)

  M T Tsuang, J R Miller, L E De Bault
• Letter: Hirschsprung's disease and congenital deafness. (1 March, 1975)

  R B Lowry