Table of contents

Research Article

• Genetic study of sample of 70 patients with myasthenia gravis. (1 December, 1968)

  A Jacob, E R Clack, A E Emery
• Incidence of fibrocystic disease in Wessex. (1 December, 1968)

  B D Hall, M J Simpkiss
• Multiple sclerosis: discordance in three pairs of dizygotic twins. (1 December, 1968)

  W S Cendrowski
• Anhidrotic ectodermal dysplasia: autosomal dominant inheritance with palate and lip anomalies. (1 December, 1968)

  R S Rapp, W E Hodgkin
• Diagnostic and genetical aspects of tuberous sclerosis. (1 December, 1968)

  N C Nevin, W G Pearce
• Amino acid patterns in cystinuric families. (1 December, 1968)

  S Kelly, W Copeland
• Testosterone excretion rates in normal males and males with an XYY complement. (1 December, 1968)

  B T Rudd, O M Galal, M D Casey
• Familial microtia with meatal atresia in two sibships. (1 December, 1968)

  L C Ellwood, S T Winter, H Dar
• Hereditary non-spherocytic haemolytic anaemia with post-splenectomy inclusion bodies and pigmenturia caused by an unstable haemoglobin Santa Ana-beta-88 (F4) leucine--proline. (1 December, 1968)

  R W Opfell, P A Lorkin, H Lehmann
• Combination of hereditary elliptocytosis and heterozygous beta-thalassaemia: a family study. (1 December, 1968)

  M Aksoy, S Erdem
• Secretor status in asthma and hay fever. (1 December, 1968)

  M A Denborough, H J Downing
• Incidence of ABO and RH blood groups in pulmonary tuberculosis in different ethnic groups. (1 December, 1968)

  N Saha, B Banerjee
• ABO blood groups and vitiligo. (1 December, 1968)

  V N Sehgal, B Dube
• Further observations on Kell blood groups in families ascertained via a mongol propositus. (1 December, 1968)

  D A Evans, P J Wren, W T Donohoe, M F Bullen, M Lewis, H Kaita, B Chown, I Uchida
• Diverse chromosomal anomalies in a family. (1 December, 1968)

  L Atkins, C S Bartsocas, P J Porter
• Congenital microcephaly with hiatus hernia and nephrotic syndrome in two sibs. (1 December, 1968)

  W H Galloway, A P Mowat
• A large deletion of chromosome no. 1 (46,XY,1?--). (1 December, 1968)

  D Aarskog
• X-linked hydrocephalus. (1 December, 1968)

  M W Shannon, H L Nadler
• Multiple anomalies associated with a small extra metacentric autosome. (1 December, 1968)

  A B Mukherjee, M W Partington, N E Simpson, K A Walmsley
• An extra small metacentric chromosome in a mentally retarded boy. (1 December, 1968)

  J Ishmael, K M Laurence
• Males with an XYY sex chromosome complement. (1 December, 1968)

  W M Brown