Table of contents

Research Article

• X linked mental retardation. (1 June, 1991)

  I A Glass
• Localisation of the MRX3 gene for non-specific X linked mental retardation. (1 June, 1991)

  A Gedeon, B Kerr, J Mulley, G Turner
• Non-specific X linked mental retardation. (1 June, 1991)

  B Kerr, G Turner, J Mulley, A Gedeon, M Partington
• Contribution to carrier detection and genetic counselling in X linked retinoschisis. (1 June, 1991)

  J Kaplan, A Pelet, H Hentati, M Jeanpierre, M L Briard, H Journel, A Munnich, J L Dufier
• Autosomal dominant inheritance of abnormalities of the hands and feet with short palpebral fissures, variable microcephaly with learning disability, and oesophageal/duodenal atresia. (1 June, 1991)

  H G Brunner, R M Winter
• On the incidence of fits and mental retardation in tuberous sclerosis. (1 June, 1991)

  D W Webb, A E Fryer, J P Osborne
• Segregation and sporadic cases in families with Hunter's syndrome. (1 June, 1991)

  G Machill, G Barbujani, G A Danieli, F H Herrmann
• Sanfilippo syndrome type D in two adolescent sisters. (1 June, 1991)

  L Siciliano, A Fiumara, L Pavone, C Freeman, D Robertson, C P Morris, J J Hopwood, P Di Natale, S Musumeci, A L Horwitz
• The Holt-Oram syndrome. (1 June, 1991)

  J A Hurst, C M Hall, M Baraitser
• Deletion of chromosome 13 in Moebius syndrome. (1 June, 1991)

  J J Slee, R D Smart, D L Viljoen
• Maternal transmission of translocation 2;21 associated with Down's syndrome. (1 June, 1991)

  S V Kotwaliwale, V V Dicholkar, N D Motashaw
• Non-penetrance in tuberous sclerosis. (1 June, 1991)

  D W Webb, J P Osborne
• A fertile male with cystic fibrosis: molecular genetic analysis. (1 June, 1991)

  C Barreto, L M Pinto, A Duarte, J Lavinha, M Ramsay
• Cranioectodermal dysplasia in sibs. (1 June, 1991)

  G D Lang, I D Young
• Partial trisomy 13q resulting from a paternal reciprocal Yq;13q translocation. (1 June, 1991)

  J Nikolis, K Ivanović, V Diklić
• Translocation 19;Y in a child with Bannayan-Zonana phenotype. (1 June, 1991)

  J Israel, M Lessick, K Szego, P Wong
• Genes for intelligence on the X chromosome. (1 June, 1991)

  G Turner, M W Partington
• X linked complicated spastic paraplegia, MASA syndrome, and X linked hydrocephalus owing to congenital stenosis of the aqueduct of Sylvius: variable expression of the same mutation at Xq28. (1 June, 1991)

  J P Fryns, A Spaepen, J J Cassiman, H van den Berghe