Table of contents

Research Article

• The French Wilms' tumour study: no clear evidence for cancer prone families. (1 June, 1994)

  C Moutou, J Hochez, A Chompret, M F Tournade, C Le Bihan, J M Zucker, J Lemerle, C Bonaïti-Pellié
• Charcot-Marie-Tooth disease in northern Sweden: pedigree analysis and the presence of the duplication in chromosome 17p11.2. (1 June, 1994)

  B H Holmberg, G Holmgren, E Nelis, C van Broeckhoven, B Westerberg
• Presymptomatic diagnosis in families with adenomatous polyposis using highly polymorphic dinucleotide CA repeat markers flanking the APC gene. (1 June, 1994)

  W A Eckert, C Jung, G Wolff
• The use of loss of constitutional heterozygosity data to ascertain the location of predisposing genes in cancer families. (1 June, 1994)

  M D Teare, K Rohde, M F Santibáñez Koref
• Segregation analysis of Alagille syndrome. (1 June, 1994)

  S Dhorne-Pollet, J F Deleuze, M Hadchouel, C Bonaïti-Pellié
• Cowden syndrome and Lhermitte-Duclos disease in a family: a single genetic syndrome with pleiotropy? (1 June, 1994)

  C Eng, V Murday, S Seal, S Mohammed, S V Hodgson, M A Chaudary, I S Fentiman, B A Ponder, R A Eeles
• Phenotypic analysis of triphalangeal thumb and associated hand malformations. (1 June, 1994)

  J Zguricas, P J Snijders, S E Hovius, P Heutink, B A Oostra, D Lindhout
• Genital tract function in men with Noonan syndrome. (1 June, 1994)

  M M Elsawi, J P Pryor, G Klufio, C Barnes, M A Patton
• The Denys-Drash syndrome. (1 June, 1994)

  R F Mueller
• A male with a de novo translocation involving loss of 15q11q13 material and Prader-Willi syndrome. (1 June, 1994)

  S Vickers, M Dahlitz, C Hardy, M Kilpatrick, T Webb
• Meckel syndrome: what are the minimum diagnostic criteria? (1 June, 1994)

  C Wright, R Healicon, C English, J Burn
• Costello syndrome: natural history and differential diagnosis of cutis laxa. (1 June, 1994)

  S J Davies, H E Hughes
• Four cases of bladder exstrophy in two families. (1 June, 1994)

  E J Messelink, D C Aronson, M Knuist, H A Heij, A Vos
• Unusual inheritance of primary ciliary dyskinesia (Kartagener's syndrome). (1 June, 1994)

  D Narayan, S N Krishnan, M Upender, T S Ravikumar, M J Mahoney, T F Dolan, A S Teebi, G G Haddad
• A further patient with Pai syndrome with autosomal dominant inheritance? (1 June, 1994)

  S Rudnik-Schöneborn, K Zerres
• Null alleles of the aldolase B gene in patients with hereditary fructose intolerance. (1 June, 1994)

  M Ali, G Tunçman, N C Cross, M Vidailhet, I Bökesoy, R Gitzelmann, T M Cox
• An inherited dystrophin deletion without muscle weakness. (1 June, 1994)

  A L Collins, K G Leyland, C R Kennedy, D Robinson, H C Spratt
• The newly recognised skeletogenital syndrome. (1 June, 1994)

  T I Farag