Table of contents

Research Article

• Xq- Turner's syndrome: reconsideration of hypothesis that Xp- causes somatic features in Turner's syndrome. (1 March, 1970)

  F Hecht, D L Jones, M Delay, H Klevit
• Genetic factors influencing human serum trehalase activity. (1 March, 1970)

  L C Eze, M C Tweedie, D A Evans
• Absent IgA and deletions of chromosome 18. (1 March, 1970)

  J M Stewart, S Go, E Ellis, A Robinson
• Affected parent and age of onset in Huntington's chorea. (1 March, 1970)

  M B Jones, C R Phillips
• Severe achondroplasia: demonstration of probable heterogeneity within this clinical syndrome. (1 March, 1970)

  D C Wallace, L A Exton, D A Pritchard, Y Leung, R A Cooke
• Congenital adrenal hypoplasia--an X-linked disease. (1 March, 1970)

  L Weiss, R C Mellinger
• A deleted B chromosome in a mosaic mother and her cri du chat progeny. (1 March, 1970)

  J Philip, N J Brandt, B Friis-Hansen, M Mikkelsen, I Tygstrup
• A family with a large Y chromosome. (1 March, 1970)

  O S el-Alfi
• Huntington's chorea. Report of a chinese family in Singapore. (1 March, 1970)

  C H Tay
• Prevalence of abnormal haemoglobins in pulmonary tuberculosis in three different ethnic groups. (1 March, 1970)

  N Saha
• Thalassaemia intermedia: a genetic study in 11 patients. (1 March, 1970)

  M Aksoy
• ABO and Rh blood groups in relation to marital status and childlessness in blood donors. (1 March, 1970)

  T M Allan
• ABO blood groups, haemoglobin genotypes, and loiasis. (1 March, 1970)

  E O Ogunba
• Inherited pericentric inversion of a human Y chromosome in trisomic Down's syndrome. (1 March, 1970)

  R S Sparkes, H M Muller, I C Veomett
• Achondroplasia and Down's syndrome. (1 March, 1970)

  A Sommer, A P Eaton
• Down's syndrome and acute leukaemia: a cytogenetic study. (1 March, 1970)

  J G Buchanan, D M Becroft
• Trisomy E and T-E fistula. (1 March, 1970)

  A Sommer, J L Grosfeld
• New human double trisomy or tetrasomy. (1 March, 1970)

  R K Dhadial
• A 46,XX,t(Cp+;Cq-) translocation in a girl with multiple congenital anomalies and in her phenotypically normal father 46,XY,t(Cq+;Cq-). (1 March, 1970)

  G J Bargman, R L Neu, H O Powers, L I Gardner
• t(2q-; Dq+) in a mentally retarded female child. (1 March, 1970)

  B C Davison, J Bedford, W Dunn
• A female with the 48,XXXX karyotype. (1 March, 1970)

  M I Berkeley, M J Faed
• Median facial cleft associated with ring E chromosome. (1 March, 1970)

  K W Dumars, L G Carnahan, R V Barrett
• Autosomal deletion syndrome 46,XX,18p-: a new case report with absence of IgA in serum. (1 March, 1970)

  P Fischer, E Golob, F Friedrich, E Kunze-Mühl, W Doleschel, H Aichmair
• 48,XY,21+, mar+mat: a case of trisomy 21 associated with an inherited small marker chromosome. (1 March, 1970)

  G J Bargman, R L Neu, H O Powers, L I Gardner