Table of contents

Research Article

• Screening of deletions in the dystrophin gene with the cDNA probes Cf23a, Cf56a, and Cf115. (1 March, 1990)

  M R Passos-Bueno, D Rapaport, D Love, T Flint, E R Bortolini, M Zatz, K E Davies
• A Chinese familial growth hormone deficiency with a deletion of 7.1 kb of DNA. (1 March, 1990)

  Y A He, S S Chen, Y X Wang, X Y Lin, D F Wang
• Small marker chromosomes in man: origin from pericentric heterochromatin of chromosomes 1, 9, and 16. (1 March, 1990)

  D F Callen, M L Ringenbergs, J C Fowler, C J Freemantle, E A Haan
• Cranial hemihypertrophy and neurodevelopmental prognosis. (1 March, 1990)

  J C Dean, G F Cole, R E Appleton, J Burn, S A Roberts, D Donnai
• EEC syndrome without ectrodactyly: report of two new families. (1 March, 1990)

  J P Fryns, E Legius, A M Dereymaeker, H Van den Berghe
• Oculodentodigital dysplasia and type III syndactyly: separate genetic entities or disease spectrum? (1 March, 1990)

  L A Brueton, S M Huson, B Farren, R M Winter
• Pontobulbar palsy and neurosensory deafness (Brown-Vialetto-Van Laere syndrome) with possible autosomal dominant inheritance. (1 March, 1990)

  S A Hawkins, N C Nevin, A E Harding
• Focal dermal hypoplasia (Goltz syndrome). (1 March, 1990)

  I K Temple, P MacDowall, M Baraitser, D J Atherton
• Multiple abnormalities in a child with partial duplications of 10p and 13q from a 3:1 segregation of a maternal t(10;13) translocation. (1 March, 1990)

  M Y Yip, J Williams, A Goddard, P Campbell, I Lambert, R W Smithells
• Microphthalmia with single central incisor and hypopituitarism. (1 March, 1990)

  H G Artman, E Boyden
• A case of atelosteogenesis. (1 March, 1990)

  K Temple, C A Hall, L Chitty, M Baraitser
• Identical twins discordant for Kallmann's syndrome. (1 March, 1990)

  L J Hipkin, I F Casson, J C Davis
• Orofaciodigital syndrome type IV (Mohr-Majewski syndrome) with severe expression expanding the known spectrum of anomalies. (1 March, 1990)

  P Meinecke, H Hayek
• Origin of the X chromosomes in a patient with the 49,XXXXY syndrome. (1 March, 1990)

  D S Plaha, D P Duckett, R A Collacott, I D Young
• Abstracts of the meeting of the Clinical Genetics Society. 5 and 6 October 1989, Middlesex. (1 March, 1990)
• Osteoglophonic dysplasia. (1 March, 1990)

  F Greenberg, R A Lewis
• Choanal atresia as a feature of ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome: a further case. (1 March, 1990)

  K Tucker, A Lipson
• Paraplegia and arthrogryposis multiplex of the lower extremities after intrauterine exposure to ergotamine. (1 March, 1990)

  A Verloes, P Emonts, M Dubois, J Rigo, J Senterre