Table of contents

Research Article

• Inheritance of congenital pyloric stenosis. (1 September, 1969)

  C O Carter, K A Evans
• A family study of atrial septal defect. (1 September, 1969)

  E M Williamson
• Camptodactyly, cleft palate, and club foot. A syndrome showing the autosomal-dominant pattern of inheritance. (1 September, 1969)

  H Gordon, D Davies, M Berman
• Apple peel syndrome (congenital intestinal atresia): a family study of seven index patients. (1 September, 1969)

  H Blyth, J A Dickson
• Inhibition of the motility of gill cilia of Dreissensia by plasma of cystic fibrosis patients and their parents. (1 September, 1969)

  G T Besley, A D Patrick, A P Norman
• G6PD deficiency in two autochthonous Croatian families. (1 September, 1969)

  D Juricić, V Vince-Ribarić, I Ruzdić, S Vuletić
• G6PD deficiency and favism in the island of Rhodes (Greece). (1 September, 1969)

  C A Kattamis, A Chaidas, S Chaidas
• Incidence of G6PD deficiency in patients of three different ethnic groups suffering from pulmonary tuberculosis. (1 September, 1969)

  N Saha
• Plasma corticosteroids in healthy twin pairs. (1 September, 1969)

  J D Maxwell, J A Boyle, W R Greig, W W Buchanan
• A cytogenetic study of familial deafness. (1 September, 1969)

  H Dar, S T Winter
• Parental dermotoglyphs in age-independent mongolism. (1 September, 1969)

  J H Priest
• Evidence of selection in mosaicism. (1 September, 1969)

  I H Porter, C D Brown, L A Gergosian, B A Paul
• Multiple congenital anomalies associated with a ring-D chromosome. (1 September, 1969)

  R C Juberg, M S Adams, W J Venema, M G Hart
• Retinoblastoma and deletion D (14) syndrome. (1 September, 1969)

  M G Wilson, J Melnyk, J W Towner
• E ring chromosome with persistent left superior vena cava and hypertrophic subaortic stenosis. (1 September, 1969)

  S Wald, E Engel, W E Nance, J Davies, F A Puyau, B C Sinclair-Smith
• Ring chromosomes in two infants with congenital malformations. (1 September, 1969)

  M A Varela, W H Sternberg
• Chromosome abnormalities in two cases with bilateral radial element defects. (1 September, 1969)

  M Faed, A Stewart, A J Keay
• Double autosomal trisomy (trisomy D+G) with mosaicism. (1 September, 1969)

  I H Porter, W Petersen, C D Brown
• Brachydactyly in an Indian family. (1 September, 1969)

  J Mohan
• Sjögren-Larsson syndrome in a Turkish family. (1 September, 1969)

  B S Sayli, I Erüreten, U Topuz
• Huntington's chorea in a Chinese family. (1 September, 1969)

  M T Tsuang