Table of contents

Research Article

• The molecular basis of genetic dominance. (1 February, 1994)

  A O Wilkie
• Pseudodicentric chromosome 18 diagnosed by chromosome painting and primed in situ labelling (PRINS). (1 February, 1994)

  C A Brandt, B Djernes, H Strømkjaer, M B Petersen, S Pedersen, J Hindkjaer, J Brinch-Iversen, G Bruun-Petersen
• Molecular characterisation of chromosome 4p deletions resulting in Wolf-Hirschhorn syndrome. (1 February, 1994)

  L L Estabrooks, A N Lamb, A S Aylsworth, N P Callanan, K W Rao
• Mosaicism with a normal cell line and an autosomal structural rearrangement. (1 February, 1994)

  R J Gardner, H E Dockery, P H Fitzgerald, R G Parfitt, D R Romain, N Scobie, R L Shaw, P Tumewu, A J Watt
• Diagnosis of adult polycystic kidney disease by genetic markers and ultrasonographic imaging in a voluntary family register. (1 February, 1994)

  R G Elles, K A Hodgkinson, N P Mallick, D J O'Donoghue, A P Read, S Rimmer, E A Watters, R Harris
• Microcephaly and congenital nephrotic syndrome owing to diffuse mesangial sclerosis: an autosomal recessive syndrome. (1 February, 1994)

  B Z Garty, B Eisenstein, J Sandbank, S Kaffe, R Dagan, N Gadoth
• Facial clefts in the west of Scotland in the period 1980-1984: epidemiology and genetic diagnoses. (1 February, 1994)

  D R FitzPatrick, P A Raine, J G Boorman
• Origin of a regressed myotonic dystrophy allele. (1 February, 1994)

  M Giordano, M S De Angelis, R Mutani, P M Richiardi
• Linkage disequilibrium between FD1-D9S202 haplotypes and the Friedreich's ataxia locus in a central-southern Italian population. (1 February, 1994)

  L Pianese, S Cocozza, G Campanella, I Castaldo, F Cavalcanti, G De Michele, A Filla, A Monticelli, M Munaro, E Redolfi
• Spondyloepimetaphyseal dysplasia with joint laxity (SEMDJL). (1 February, 1994)

  P Beighton
• Hydrocephalus in an infant with trisomy 22. (1 February, 1994)

  F Fahmi, S Schmerler, R G Hutcheon
• Recurrence of Pallister-Hall syndrome in two sibs. (1 February, 1994)

  H M Thomas, P J Todd, D Heaf, A E Fryer
• Acute myeloid leukaemia in a patient with Seckel syndrome. (1 February, 1994)

  A Hayani, C R Suarez, Z Molnar, M LeBeau, J Godwin
• Partial trisomy 3q causing mild Cornelia de Lange phenotype. (1 February, 1994)

  S E Holder, L M Grimsley, R W Palmer, L J Butler, M Baraitser
• Paternal pericentric inversion of chromosome 4 as a cause of recurrent pregnancy loss. (1 February, 1994)

  G C Wolf, J Mao, L Izquierdo, G Joffe
• Another patient with an interstitial deletion of chromosome 9: case report and a review of six cases with del(9)(q22q32). (1 February, 1994)

  H Y Kroes, J H Tuerlings, R Hordijk, N R Folkers, L P ten Kate
• Association of 1078 del T cystic fibrosis mutation with severe disease. (1 February, 1994)

  P Moullier, M Jéhanne, M P Audrézet, B Mercier, C Verlingue, I Quéré, H Guillermit, O Raguénès, V Storni, G Rault