Table of contents

Research Article

• Molecular genetics of neurological tumours. (1 June, 1992)

  R Y Chung, B R Seizinger
• Experience with direct molecular diagnosis of fragile X. (1 June, 1992)

  J C Mulley, S Yu, A K Gedeon, A Donnelly, G Turner, D Loesch, C J Chapman, R J Gardner, R I Richards, G R Sutherland
• Detection and characterisation of an overmodified type III collagen by analysis of non-cutaneous connective tissues in a patient with Ehlers-Danlos syndrome IV. (1 June, 1992)

  L Nuytinck, P Narcisi, A Nicholls, J P Renard, F M Pope, A De Paepe
• Linkage of autosomal dominant dystrophic epidermolysis bullosa in three British families to the marker D3S2 close to the COL7A1 locus. (1 June, 1992)

  L al-Imara, A J Richards, R A Eady, I M Leigh, M Farrall, F M Pope
• Limb-girdle type muscular dystrophy in a large family with distal myopathy: homozygous manifestation of a dominant gene? (1 June, 1992)

  B Udd
• Confirmation of an association between RFLPs at the transforming growth factor-alpha locus and non-syndromic cleft lip and palate. (1 June, 1992)

  S E Holder, G M Vintiner, B Farren, S Malcolm, R M Winter
• No evidence of linkage between the transforming growth factor-alpha gene in families with apparently autosomal dominant inheritance of cleft lip and palate. (1 June, 1992)

  G M Vintiner, S E Holder, R M Winter, S Malcolm
• Use of oocytes from anonymous, matched, fertile donors for prevention of heritable genetic diseases. (1 June, 1992)

  B J Van Voorhis, R A Williamson, J L Gerard, D G Hammitt, C H Syrop
• A complex rearrangement associated with sex reversal and the Wolf-Hirschhorn syndrome: a cytogenetic and molecular study. (1 June, 1992)

  K Coles, M Mackenzie, J Crolla, J Harvey, J Starr, F Howard, P Jacobs
• Distal 8p deletion (8p23.1----8pter): a common deletion? (1 June, 1992)

  R Hutchinson, M Wilson, L Voullaire
• Angelman syndrome. (1 June, 1992)

  J Clayton-Smith, M E Pembrey
• Ovarian cancer family and prophylactic choices. (1 June, 1992)

  D G Evans, G Ribiero, D Warrell, D Donnai
• Acromegaloid facial appearance (AFA) syndrome: report of a second family. (1 June, 1992)

  B Dallapiccola, L Zelante, L Accadia, R Mingarelli
• An infant with multiple congenital abnormalities and biochemical findings suggesting a variant of galactosialidosis. (1 June, 1992)

  B Say, F A Hommes, S A Malik, N J Carpenter
• The 3-M syndrome: risk of intracerebral aneurysm? (1 June, 1992)

  R F Mueller, J Buckler, R Arthur, G Bonsor, P Dear, K Walters, G M Towns
• Cardiofaciocutaneous syndrome with new ectodermal manifestations. (1 June, 1992)

  P D Turnpenny, J C Dean, I A Auchterlonie, A W Johnston
• Recurrence of orbital cysts in the branchio-oculo-facial syndrome. (1 June, 1992)

  D W Fielding, A E Fryer
• Terminal 22q deletion associated with a partial deficiency of arylsulphatase A. (1 June, 1992)

  K Narahara, Y Takahashi, M Murakami, K Tsuji, Y Yokoyama, R Murakami, S Ninomiya, Y Seino
• Two sibs with Wiedemann-Rautenstrauch syndrome: possibilities of prenatal diagnosis by ultrasound. (1 June, 1992)

  G Castiñeyra, M Panal, H Lopez Presas, E Goldschmidt, J M Sánchez
• The demonstration of monozygosity in twins discordant for sacral agenesis. (1 June, 1992)

  M D Crawfurd, J Cheshire, T M Wilson, C R Woodhouse
• Palmoplantar hyperkeratosis and deafness. (1 June, 1992)

  J Verbov