Table of contents

Research Article

• Medical genetics in Hungary. (1 January, 1988)

  A Czeizel
• Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome. (1 January, 1988)

  K E Davies, T J Smith, S Bundey, A P Read, T Flint, M Bell, A Speer
• Service experience using DNA analysis for genetic prediction in Duchenne muscular dystrophy. (1 January, 1988)

  J Goodship, S Malcolm, M E Robertson, M E Pembrey
• Evidence linking familial thrombosis with a defective antithrombin III gene in two British kindreds. (1 January, 1988)

  S H Sacks, J M Old, S T Reeders, D J Weatherall, A S Douglas, J H Winter, C R Rizza
• The use of restriction fragment length polymorphisms in prenatal diagnosis of dihydropteridine reductase deficiency. (1 January, 1988)

  H H Dahl, S Wake, R G Cotton, D M Danks
• Polymorphic acetylation of sulphamethazine in a Zimbabwe population. (1 January, 1988)

  C F Nhachi
• Osteoporosis-pseudoglioma syndrome with congenital heart disease: a new association. (1 January, 1988)

  A S Teebi, S A Al-Awadi, M J Marafie, R A Bushnaq, S Satyanath
• Association of syndactyly, ectodermal dysplasia, and cleft lip and palate: report of two sibs from Turkey. (1 January, 1988)

  G Oğur, M Yüksel
• Iris coloboma, ptosis, hypertelorism, and mental retardation: a new syndrome. (1 January, 1988)

  M Baraitser, R M Winter
• Association of an ataxia indistinguishable from Friedreich's ataxia and congenital glaucoma in a family: a new syndrome. (1 January, 1988)

  O Combarros, J Calleja, C Leno, J Berciano
• Blepharophimosis, ptosis, epicanthus inversus syndrome (BPES syndrome) (1 January, 1988)

  C Oley, M Baraitser
• Prenatal diagnosis of inv(X)(q12q28) in a male fetus. (1 January, 1988)

  R L Neu, H S Brar, B J Koos
• A recognisable short stature syndrome with premature aging and pigmented naevi. (1 January, 1988)

  M Baraitser, J Insley, R M Winter
• VATER association: report of a case with three unreported malformations. (1 January, 1988)

  M Dusmet, F Fête, A Crusi, J N Cox
• Two whole arm reciprocal translocations. (1 January, 1988)

  A Smith, R Murray, G den Dulk
• Royal Society discussion meeting: Prevention and Avoidance of Genetic Disease, held on 29 to 30 April 1987 at the Royal Society. (1 January, 1988)

  N Haites, A W Johnston
• Expression of fragile X chromosome and possible deletion in successive cell divisions. (1 January, 1988)

  Z Laća, S Branković
• Noonan syndrome. (1 January, 1988)

  A E Lin
• The population genetics of Duchenne muscular dystrophy. (1 January, 1988)

  J H Edwards