Table of contents

Research Article

• A rare blood group antigen An a (Ahonen). (1 December, 1972)

  U Furuhjelm, H R Nevanlinna, J Gavin, R Sanger
• The Dombrock system: linkage relations with other blood group loci. (1 December, 1972)

  P Tippett, J Gavin, R Sanger
• Christmas disease in one of a pair of monozygotic twin girls, possibly the effect of lyonization. (1 December, 1972)

  T Révész, D Schuler, B Goldschmidt, S Elödi
• A new genetic variant of the spinal muscular atrophies in infancy. (1 December, 1972)

  H Zellweger, E Hanhart, H J Schneider
• Pedigrees with diabetes insipidus, diabetes mellitus, and optic atrophy. (1 December, 1972)

  J H Sunder, T S Danowski, F M Kenny, R C Khurana, A Sun, S Nolan, T Stephan
• Pericentric enversion of chromosome no. 13 in a large family leading to duplication deficiency causing congenital malformations in three individuals. (1 December, 1972)

  H Hauksdóttir, S Halldórsson, O Jensson, M Mikkelsen, A McDermott
• Reciprocal chromosome translocations: analysis of two mutants by interactive computer. (1 December, 1972)

  R W Dickerson, N H Xuong, O W Jones
• The nature and inheritance of Kirner's deformity. (1 December, 1972)

  T J David, R L Burwood
• Erythrocyte acid phosphatase polymorphism and haemolysis. (1 December, 1972)

  E Bottini, P Lucarelli, V Bastianon, F Gloria
• Haemoglobin Q India (alpha 64(E13) aspartic acid histidine) associated with beta-thalassemia observed in three Sindhi families. (1 December, 1972)

  P K Sukumaran, S M Merchant, M P Desai, B G Wiltshire, H Lehmann
• Palmar dermatoglyphs in tuberous sclerosis. (1 December, 1972)

  T J David
• The effect of absence of thumb on palmar dermatoglyphics. (1 December, 1972)

  S B Holt
• Familial cancer of the colon and rectum. (1 December, 1972)

  G H Dunstone, T W Knaggs
• Apparent G-monosomy, G-deletion, and incomplete Down's syndrome in a single family. (1 December, 1972)

  R Schmidt, G Mundel, M Rosenblatt, M B Katznelson
• Trisomy-18 syndrome caused by translocation or isochromosome formation. A case report with bibliography. (1 December, 1972)

  H Müller, E M Bühler, E Signer, F Egli, G R Stalder
• Congenital leukaemia with 46,XX,t(Bq+,Cq-) cells. (1 December, 1972)

  H Van den Berghe, J P Fryns, H Verresen
• Ring F chromosome mosaicism (46,XY,20r-46,XY) in an epileptic child without apparent haematological disease. (1 December, 1972)

  M Faed, H G Morton, J Robertson
• Bone marrow chromosomes in Fanconi's anaemia. (1 December, 1972)

  S R Wolman, M Swift
• Fanconi's anaemia: report of a patient with significant chromosomal abnormalities in bone marrow cells. (1 December, 1972)

  M J Shahid, F P Khouri, S K Ballas
• Down's syndrome with an atypical G-G translocation derived from familial pericentric inversion in one chromosome of the G group. (1 December, 1972)

  S Morić-Petrović, Z Laća, P Kalicanin
• A new HGPRT-deficient phenotype? (1 December, 1972)

  S Kelly, E J Hart, L Desjardins