Table of contents

Research Article

• Cloning of the human alpha 1 antichymotrypsin gene and genetic analysis of the gene in relation to alpha 1 antitrypsin deficiency. (1 June, 1988) Free

  G D Kelsey, D Abeliovich, C J McMahon, D Whitehouse, G Corney, S Povey, D A Hopkinson, J Wolfe, G Mieli-Vergani, A P Mowat
• Partial gene duplication in Duchenne and Becker muscular dystrophies. (1 June, 1988) Free

  X Y Hu, A H Burghes, P N Ray, M W Thompson, E G Murphy, R G Worton
• Inherited deletion of subband Xp21.13 in a male with Duchenne muscular dystrophy. (1 June, 1988) Free

  W Werner, A W Spiegler
• Recognition and reanalysis of a cell line from a manifesting female with X linked hypohidrotic ectodermal dysplasia and an X; autosome balanced translocation. (1 June, 1988) Free

  J Zonana, S H Roberts, N S Thomas, P S Harper
• C4 null phenotypes among lupus erythematosus patients are predominantly the result of deletions covering C4 and closely linked 21-hydroxylase A genes. (1 June, 1988) Free

  J Partanen, S Koskimies, E Johansson
• A developing role in genetic counselling. (1 June, 1988) Free

  S Farnish
• Birth defects following maternal exposure to ergotamine, beta blockers, and caffeine. (1 June, 1988) Free

  H E Hughes, D A Goldstein
• New autosomal recessive faciodigitogenital syndrome. (1 June, 1988) Free

  A S Teebi, K K Naguib, S Al-Awadi, Q A Al-Saleh
• Clinical features and reproductive patterns in fragile X female heterozygotes. (1 June, 1988) Free

  D Z Loesch, D A Hay
• Type I Gaucher disease. (1 June, 1988) Free

  J Goldblatt
• The influence of culture media on chromosome aberration levels, sister chromatid exchange frequencies, and the rate of cell proliferation: comparison of Iscove's low folate medium with Eagle's MEM. (1 June, 1988) Free

  E J Tawn, R Earl
• John Dalton (1766-1844). (1 June, 1988) Free

  A E Emery
• Translocation (1;22) in a child with bilateral oblique facial clefts. (1 June, 1988) Free

  M Dasouki, M Barr, R P Erickson, B Cox
• Oculotrichodysplasia (OTD): a new probably autosomal recessive condition. (1 June, 1988) Free

  L Cecatto-De-Lima, M Pinheiro, N Freire-Maia