Table of contents

Articles

• Myoglobin in Primary Muscular Disease: I. Duchenne Muscular Dystrophy: and: II. Muscular Dystrophy of Distal Type (1 December, 1973)

  A. E. Romero-Herrera, H. Lehmann, B. E. Tomlinson, J. N. Walton
• A `New' Saliva Substance, Probably Inherited, and Serologically Independent of ABH, Lewis, and Sd^a Blood Group Substances

  (1 December, 1973)

  P. Balding, E. R. Gold
• Parental Dermatoglyphics in Down's Syndrome. A Ten-year Study (1 December, 1973)

  J. H. Priest, C. Verhulst, S. Sirkin
• The Relation of Sex of Affected Parent to the Age at Onset of Huntington's Disease (1 December, 1973)

  C. J. Brackenridge
• Hirschsprung's Disease and Congenital Deafness (1 December, 1973)

  Rosalind Skinner, David Irvine
• Genetic Association in Myocardial Infarction: Ethnicity; ABO, Rh, Le^a, Xg^a Blood Groups; G6PD Deficiency; and Abnormal Haemoglobins

  (1 December, 1973)

  N. Saha, C. C. S. Toh, M. B. Ghosh
• Lip Pits and Congenital Absence of Second Premolars: Varied Expression of the Lip Pits Syndrome (1 December, 1973)

  Edward L. Schneider
• Fluorescence and Autoradiographic Studies in Patients with Turner's Syndrome and 46,XXp— and 46,XXq— Karyotypes (1 December, 1973)

  K. Boczkowski, Margareta Mikkelsen
• D/D Translocations in Males Examined for Military Service (1 December, 1973)

  Eva Zeuthen, Johannes Nielsen
• Segregation Analysis of A Large t(21q22q) Family (1 December, 1973)

  C. J. Chapman, R. J. M. Gardner, A. M. O. Veale
• Antenatal Diagnosis of Patau's Syndrome (Trisomy 13) including a Detailed Pathological Study of the Fetus (1 December, 1973)

  L. J. Butler, H. E. Reiss, N. E. France, Sylvia Briddon
• Sibship (21q21q) Translocation Down's Syndrome with Maternal Transmission (1 December, 1973)

  M. Furbetta, A. Falorni, P. Antignani, A. Cao