Table of contents

Research Article

• Attitudes of patients and their relatives to Huntington's disease. (1 September, 1975)

  R Stern, R Eldridge
• Variability of acid hydrolase activities in cultured skin fibroblasts and amniotic fluid cells. (1 September, 1975)

  E Young, P Willcox, A E Whitfield, A D Patrick
• Transplacental passage of blood cells. (1 September, 1975)

  J Schröder
• Development of dermal ridges in the fetus. (1 September, 1975)

  M Okajima
• Specific chromosome aberrations in ataxia telangiectasia. (1 September, 1975)

  J M Oxford, D G Harnden, J M Parrington, J D Delhanty
• Alpha1-antitrypsin phenotypes in sex chromosome mosaicism. (1 September, 1975)

  F Kueppers, P O'Brien, E Passarge, H W Rüdiger
• Identification of C trisomies in human abortuses. (1 September, 1975)

  J Boué, A Boué, C Deluchat, N Perraudin, F Yvert
• Homozygous haemoglobin D Punjab. (1 September, 1975)

  C Politis-Tsegos, P Kynoch, A Lang, H Lehmann, P A Lorkin, R Stathopoulou, G Wakefield
• Haemoglobin Lepore in Cyprus. (1 September, 1975)

  Z Zachariadis, P E Nute, G Stamatoyannopoulos
• Congenital vertebral anomalies: aetiology and relationship to spina bifida cystica. (1 September, 1975)

  R Wynne-Davies
• Ocular colobomata, cardiac defect, and other anomalies: a study of seven cases including two sibs. (1 September, 1975)

  C K Ho, R L Kaufman, S M Podos
• Haemoglobin Hasharon in a north Italian community. (1 September, 1975)

  R Alberti, G M Mariuzzi, M Marinucci, E Bruni, L Tenteri
• A new case of haemoglobin Bucuresti in a Cuban family: further functional studies. (1 September, 1975)

  B Colombe, M P Benitez, L Bernini, J Elien, H Wajeman, D Labie
• Klinefelter's syndrome associated with a D/D translocation. (1 September, 1975)

  M Sparagana, G P Smith
• Partial 9 trisomy by 3:1 segregation of balanced maternal translocation (7q+; 9q-). (1 September, 1975)

  V B Penehaszadeh, R Coco
• Pseudohermaphroditism with clinical features of trisomy 19 in an infant trisomic for parts of chromosomes 16 and 18: 47,XY,der(18),t(16;18)(p12;q11)mat. (1 September, 1975)

  L M Stern, A R Mureh
• A syndrome of hypohidrotic ectodermal dysplasia with normal teeth, peculiar facies, pigmentary disturbances, psychomotor and growth retardation, bilateral nuclear cataract, and other signs. (1 September, 1975)

  N Freire-Maia, V A Fortes, L C Pereira, J M Opitz, F A Marcalle, I J Cavalli
• A case of partial (9p) trisomy in a family with a balanced translocation 46,XX,t(1p+9q-). (1 September, 1975)

  M K Mason, D A Spencer, A Rutter