Table of contents

Research Article

• Syndrome of retardation with urogenital and skeletal anomalies (Smith-Lemli-Opitz syndrome): clinical features and mode of inheritance. (1 June, 1969)

  L Dallaire
• An association of Rh type and gynaecological disease with twinning. (1 June, 1969)

  F V De George
• Hypertrophic pyloric stenosis: adult and congenital types occurring in the same family. (1 June, 1969)

  C Zavala, A Bolio, R Montalvo, R Lisker
• Inheritance of coeliac disease. (1 June, 1969)

  W M McCrae
• Hearing impairment in female carriers of the sex-linked syndrome of deafness with albinism. (1 June, 1969)

  K Fried, M Feinmesser, J Tsitsianov
• Mongolism and maternal menarche. (1 June, 1969)

  J M Berg, J T Bavin
• Consistent and variable chromosome anomalies in parents of children with Down's syndrome. (1 June, 1969)

  J Kahn, K Abe
• Studies on glucose-6-phosphate dehydrogenase deficient Egyptian families. (1 June, 1969)

  N Hashem, A Nour
• Comparison of strength of isoagglutinin titres in English and Finnish populations. (1 June, 1969)

  I J Seppälä
• XYY syndrome, and XYY-XXYY mosaicism also showing features of Klinefelter's syndrome. (1 June, 1969)

  D A Spencer, J W Eyles, M K Mason
• Translocations of D chromosomes in two families: t(13q14q) and t(13q14q)+(13p14p). (1 June, 1969)

  C G Palmer, P M Conneally, J C Christian
• Familial transmission of a chromosomal translocation t(2q+;Cp-). (1 June, 1969)

  C B Lozzio, A A Kattine
• Welshness and fertility. (1 June, 1969)

  D J Ashley
• Blood groups and lung cancer. (1 June, 1969)

  D J Ashley
• A haptoglobin Johnson family with nonhypohaptoglobinaemic HpJ-Hp2. (1 June, 1969)

  J Pintera, R Dvorák, J Vacl, J Fiser
• Further evidence for close linkage of the Hb-beta and Hb-delta loci in man. (1 June, 1969)

  M K Mishu, W E Nance
• Familial jaw cysts in Charcot-Marie-Tooth disease. (1 June, 1969)

  M R Swift, S L Horowitz
• Postaxial polydactyly in three Indian families. (1 June, 1969)

  J Mohan
• Partial trisomy in a child with features suggesting mongolism. (1 June, 1969)

  H K Kumbnani, R A Pfeiffer
• 46,XY,21qi-46,XY,21p- mosaicism in a child with Down's syndrome. (1 June, 1969)

  L Atkins, M Feingold
• Double autosomal trisomy and mosaicism for three cell lines in man: coexisting trisomy 13-15, trisomy 17-18, and a minority cell line trisomic for a chromosome of both groups. (1 June, 1969)

  O M Garson, A G Baikie, J Ferguson, C H Greer
• A patient with a short arm deletion of chromosome 18 (46,XY,18p-). (1 June, 1969)

  L Weiss, K Mayeda
• A patient with 45,XX,Gminus-46,XX,Gr mosaicism. (1 June, 1969)

  C E Blank, J Lorber
• Congenital malformations associated with a ring 4 chromosome. (1 June, 1969)

  R Carter, E Baker, D Hayman