Table of contents

Research Article

• DNA prediction in cystic fibrosis. (1 August, 1986)

  P S Harper
• The Van der Woude syndrome (dominantly inherited lip pits and clefts). (1 August, 1986)

  A Schinzel, M Kläusler
• Cystic fibrosis carrier detection using a linked gene probe. (1 August, 1986)

  M Farrall, P Scambler, K W Klinger, K Davies, C Worrall, R Williamson, B Wainwright
• Application of three intragenic DNA polymorphisms for carrier detection in haemophilia B. (1 August, 1986)

  J M Connor, A F Pettigrew, C Shiach, I M Hann, G D Lowe, C D Forbes
• Phenotype-karyotype correlation in patients trisomic for various segments of chromosome 13. (1 August, 1986)

  S A Tharapel, R C Lewandowski, A T Tharapel, R S Wilroy
• Risk estimation in autosomal dominant disorders with reduced penetrance. (1 August, 1986)

  A E Emery
• Genetic heterogeneity in Gaucher disease. (1 August, 1986)

  J Zlotogora, R Zaizov, C Klibansky, Y Matoth, G Bach, T Cohen
• Differentiation of heterozygotes in recessive albinism. (1 August, 1986)

  D F Roberts, J G Kromberg, T Jenkins
• The birth prevalence rates for the skeletal dysplasias. (1 August, 1986)

  I M Orioli, E E Castilla, J G Barbosa-Neto
• Aetiological factors in hypospadias. (1 August, 1986)

  E Calzolari, M R Contiero, E Roncarati, P L Mattiuz, S Volpato
• Ratio of crown-rump distance to total length in preterm and term infants. (1 August, 1986)

  P Merlob, Y Sivan, S H Reisner
• A paracentric inversion of 7q illustrating a possible interchromosomal effect. (1 August, 1986)

  J L Watt, K Ward, D A Couzin, G S Stephen, A Hill
• Autosomal dominant thoracolaryngopelvic dysplasia: Barnes syndrome. (1 August, 1986)

  J Burn, C Hall, D Marsden, D J Matthew
• Robinow syndrome without mesomelic 'brachymelia': a report of five cases. (1 August, 1986)

  M D Bain, R M Winter, J Burn
• Microcephaly, short stature, and developmental delay associated with a chemotactic defect and transient hypogammaglobulinaemia in two brothers. (1 August, 1986)

  B Say, N Barber, G C Miller, S E Grogg
• Megacystis-microcolon-intestinal hypoperistalsis syndrome: confirmation of autosomal recessive inheritance. (1 August, 1986)

  R M Winter, S A Knowles
• Monozygotic twins concordant for congenital short femur. (1 August, 1986)

  J M Connor, P S Rae, R A Connor
• Poland syndrome associated with 'morning glory' syndrome (coloboma of the optic disc). (1 August, 1986)

  D T Pisteljić, D Vranjesević, S Apostolski, D D Pisteljić
• Interstitial deletion of chromosome 4q diagnosed prenatally. (1 August, 1986)

  J M Campbell, J Williams, G Batcup
• A case of de novo, double, balanced translocations (distal 9p to 3p, distal 18q to 3q). (1 August, 1986)

  J E Hall, E J Hart
• Pregnancy wastage associated with paracentric inversion of chromosome 13. (1 August, 1986)

  B G Bateman, R Neu, W C Nunley, T E Kelly
• A pericentric inversion duplication of the subcentromeric region of chromosome 12q. (1 August, 1986)

  A P Albert, J Holdsworth, C Massyn
• Partial trisomy 1q25----qter. (1 August, 1986)

  E J Tawn, M B Roberts, R G Ghazala, E M Pyta
• Secondary amenorrhoea and 47,XX,i(Xq) karyotype. (1 August, 1986)

  T E Kelly, J W Wilks, H E Wyandt
• Necropsy findings in a child with FG syndrome. (1 August, 1986)

  E M Thompson, B N Harding, B D Lake, S C Smith
• DNA probes or microvillar enzymes or both for prenatal diagnosis of cystic fibrosis. (1 August, 1986)

  D J Brock
• Clinical features of homozygous alpha 2(I) collagen deficient osteogenesis imperfecta. (1 August, 1986)

  F M Pope, A C Nicolls, G Osse, K W Lee