Table of contents

Research Article

• A new syndrome of autosomal recessive nephropathy, deafness, and hyperparathyroidism. (1 May, 1989)

  B D Edwards, M A Patton, S A Dilly, J B Eastwood
• Fertility in a male with trisomy 21. (1 May, 1989)

  R Sheridan, J Llerena, S Matkins, P Debenham, A Cawood, M Bobrow
• Benign muscular dystrophy: risk calculation in families with consanguinity. (1 May, 1989)

  G Wolff, C R Müller, T Grimm
• X linked or autosomal recessive? A new approach to an old problem. (1 May, 1989)

  A P Read
• Further evidence localising the gene for Hunter's syndrome to the distal region of the X chromosome long arm. (1 May, 1989)

  S H Roberts, M Upadhyaya, M Sarfarazi, P S Harper
• Exclusion of the COL2A1 gene as the mutation site in diastrophic dysplasia. (1 May, 1989)

  K Elima, I Kaitila, L Mikonoja, U Elonsalo, L Peltonen, E Vuorio
• Moore-Federman syndrome and acromicric dysplasia: are they the same entity? (1 May, 1989)

  R M Winter, M A Patton, J Challener, R F Mueller, M Baraitser
• Neural tube defect recurrence after 'partial' vitamin supplementation. (1 May, 1989)

  S Sheppard, N C Nevin, M J Seller, J Wild, R W Smithells, A P Read, R Harris, D W Fielding, C J Schorah
• Y chromosome specific probes identify breakpoint in a 45,X/46,X,del(Y)(pter----q11.1:) karyotype of an infertile male. (1 May, 1989)

  G C Beverstock, J D MacFarlane, H Veenema, H Hoekman, P J Goodfellow
• Toluene embryopathy: two new cases. (1 May, 1989)

  J H Hersh
• Synchrony of oculocutaneous albinism, the Prader-Willi syndrome, and a normal karyotype. (1 May, 1989)

  C E Wallis, P H Beighton
• A new recessive syndrome of unusual facies, digital abnormalities, and ichthyosis. (1 May, 1989)

  J Clayton-Smith, D Donnai
• Deletion (12)(q15q21.2). (1 May, 1989)

  M S Watson, L McAllister-Barton, M J Mahoney, W R Breg
• A third case of de novo partial trisomy 4p. (1 May, 1989)

  J W Oorthuys, K B Gerssen-Schoorl, J M de Pater, H F de France
• Short rib syndrome without polydactyly. (1 May, 1989)

  K Chen, P A McKeever, I D Young
• Van der Woude syndrome and limb defects: the chance of recurrence. (1 May, 1989)

  A Lipson
• Fetal valproate phenotype is recognisable by mid pregnancy. (1 May, 1989)

  F Serville, D Carles, S Guibaud, D Dallay