Table of contents

Research Article

• Polycystic disease of kidney and liver presenting in childhood. (1 September, 1971)

  H Blyth, B G Ockenden
• Polycystic kidneys associated with malformations of the brain, polydactyly, and other birth defects in newborn sibs. A lethal syndrome showing the autosomal-recessive pattern of inheritance. (1 September, 1971)

  K Fried, E Liban, M Lurie, S Friedman, S H Reisner
• X-linked spondyloepiphyseal dysplasia tarda: clinical and linkage data. (1 September, 1971)

  R M Bannerman, G B Ingall, J F Mohn
• Haemoglobin Osu-Christiansborg: a new beta-chain variant of haemoglobin A ( beta52 (D3) aspartic acid leads to asparagine) in combination with haemoglobin S. (1 September, 1971)

  F I Konotey-Ahulu, J L Kinderlerer, H Lehmann, B Ringelhann
• Differentiation of two genetically specific types of depression by the response to antidepressant drugs. (1 September, 1971)

  C M Pare, J W Mack
• Mutation rate in Duchenne muscular dystrophy. (1 September, 1971)

  H K Goswami, B D Chaurasia
• Familial total anomalous pulmonary venous return. (1 September, 1971)

  J E Paz, E E Castilla
• Distribution of ABO blood groups, G6PD deficiency, and abnormal haemoglobins in leprosy. (1 September, 1971)

  N Saha, H B Wong, B Banerjee, M O Wong
• Rh immunization following incompatible blood transfusion and a possible long-term complication of anti-D immunoglobulin therapy. (1 September, 1971)

  M E Beard, J Pemberton, J Blagdon, W F Jenkins
• Suppression of the immune response. (1 September, 1971)

  J Bradley, C J Elson
• Group G deletion syndromes. (1 September, 1971)

  R P Kelch, M Franklin, R D Schmickel
• The inheritance of a structural anomaly of one chromosome No. 16 in a kindred (46,16-,C+). (1 September, 1971)

  J Chemke, A Robinson
• The 13q- deletion syndrome. (1 September, 1971)

  E Grace, J Drennan, D Colver, R R Gordon
• Somatic stigmata of Turner's syndrome in a patient with 46,XXq-. (1 September, 1971)

  M Bocian, E Krmpotic, K Szego, I M Rosenthal
• Klinefelter's syndrome and G trisomy. (1 September, 1971)

  B Erdtmann, A A de Freitas, R P de Souza, F M Salzano
• A case of cri-du-chat associated with cataracts and transmitted from a mother with a 4-5 translocation. (1 September, 1971)

  H Grotsky, L Y Hsu, K Hirschhorn
• A prisoner with an unusual karyotype (46,XY,Dq-). (1 September, 1971)

  J Kahn, F Reed
• Partial deletion of a group-F (19-20) chromosome in a physically handicapped psychiatric male patient. (1 September, 1971)

  P Genest, M Bouchard, J Poty
• An extra small metacentric autosome in a mentally retarded boy with multiple malformations. (1 September, 1971)

  S Armendares, L Buentello, F Salamanca
• An extra small metacentric chromosome in association with multiple congenital abnormalities. (1 September, 1971)

  W H Finley, S C Finley, D Monsky
• Trisomy D-trisomy E mosaicism in an infant male. (1 September, 1971)

  R J Warren, J I Keith
• X chromosome long arm deletion in a patient with Down's syndrome. (1 September, 1971)

  F W Luthardt, C G Palmer
• Trisomy 18 in one of fraternal twins. (1 September, 1971)

  D Gertzer, G Nathenson