Table of contents

Research Article

• Familial XY gonadal dysgenesis. (1 June, 1970)

  J Chemke, R Carmichael, J M Stewart, R H Geer, A Robinson
• Relation of face shape to susceptibility to congenital cleft lip. A preliminary report. (1 June, 1970)

  F C Fraser, H Pashayan
• Chromosome abnormalities in early spontaneous abortions. (1 June, 1970)

  D T Arakaki, S H Waxman
• Dermatoglyphs in leukaemia. (1 June, 1970)

  J L Verbov
• Trisomy 13 syndrome in Chinese infants. Clinical findings and incidence. (1 June, 1970)

  F C Yu, L T Gutman, S W Huang, J W Fresh, I Emanuel
• Trisomy 18 syndrome in Chinese infants. Clinical findings and incidence. (1 June, 1970)

  I Emanuel, S W Huang, W T Chiang, C P Yang
• Significance of chromosome 17ps+ in three generations of a family. (1 June, 1970)

  J H Priest, D C Peakman, S R Patil, A Robinson
• Familial occurrence of a small, supernumerary metacentric chromosome in phenotypically normal women. (1 June, 1970)

  M A Ridler, J M Berg, M J Pendrey, P Saldaña, J A Timothy
• Recessive albinism in three children and both parents. (1 June, 1970)

  M Oliver, K Fried
• Von Hippel-Lindau syndrome: a report on three kindreds. (1 June, 1970)

  M H Shokeir
• Familial hypertrichosis cubiti: hairy elbows syndrome. (1 June, 1970)

  P Beighton
• A 45,XY,5-15-,t(5q15q) cri-du-chat child. (1 June, 1970)

  L Jackson, M Barr
• Wolf-Hirschhorn syndrome associated with an unusual abnormality of chromosome no. 4. (1 June, 1970)

  M G Wilson, J W Towner, L D Negus
• Deletion of short arm of no. 4 (4p-)--a detailed case report. (1 June, 1970)

  A R Wilcock, F G Adams, P Cooke, R R Gordon
• Familial occurrence of congenital malformations and ring chromosome (46,XX,Cr). (1 June, 1970)

  G Gacs, D Schuler, M Sellyei
• Developmental abnormalities in a patient with karyotype 46,XX,bq+. (1 June, 1970)

  J E Chakanovskis, G R Sutherland
• Hemifacial microsomia--oculo-auriculo-vertebral dysplasia. A patient with overlapping features. (1 June, 1970)

  H Pashayan, L Pinsky, F C Fraser