Table of contents

Research Article

• Implications for medical genetics of the House of Commons Science and Technology Committee's report on human genetics. (1 April, 1996)

  R Harris
• A modifying locus for familial adenomatous polyposis may be present on chromosome 1p35-p36. (1 April, 1996)

  I P Tomlinson, K Neale, I C Talbot, A D Spigelman, C B Williams, R K Phillips, W F Bodmer
• Correlation between the development of extracolonic manifestations in FAP patients and mutations beyond codon 1403 in the APC gene. (1 April, 1996)

  Z Dobbie, M Spycher, J L Mary, M Häner, I Guldenschuh, R Hürliman, R Amman, J Roth, H Müller, R J Scott
• Large scale deletions of the 5q13 region are specific to Werdnig-Hoffmann disease. (1 April, 1996)

  P Burlet, L Bürglen, O Clermont, S Lefebvre, L Viollet, A Munnich, J Melki
• The molecular defect underlying canine fucosidosis. (1 April, 1996)

  B J Skelly, D R Sargan, M E Herrtage, B G Winchester
• The dysmorphic human-mouse homology database (DHMHD): an interactive World-Wide Web resource for gene mapping. (1 April, 1996)

  C D Evans, A G Searle, A A Schinzel, R M Winter
• Complementation analysis in patients with the clinical phenotype of a generalised peroxisomal disorder. (1 April, 1996)

  S J Steinberg, A H Fensom
• Holt-Oram syndrome: a clinical genetic study. (1 April, 1996)

  R A Newbury-Ecob, R Leanage, J A Raeburn, I D Young
• Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21. (1 April, 1996)

  R H Wallace, S F Berkovic, R A Howell, G R Sutherland, J C Mulley
• Parents' responses to predictive genetic testing in their children: report of a single case study. (1 April, 1996)

  S Michie, V McDonald, M Bobrow, C McKeown, T Marteau
• Syndromes with lissencephaly. (1 April, 1996)

  D T Pilz, O W Quarrell
• A novel splice site mutation in a Becker muscular dystrophy patient. (1 April, 1996)

  C Bartolo, A C Papp, P J Snyder, M S Sedra, A H Burghes, C D Hall, J R Mendell, T W Prior
• Phenotypic expression in von Hippel-Lindau disease: correlations with germline VHL gene mutations. (1 April, 1996)

  E R Maher, A R Webster, F M Richards, J S Green, P A Crossey, S J Payne, A T Moore
• Familial cluster of ovarian small cell carcinoma: a new mendelian entity? (1 April, 1996)

  M Longy, C Toulouse, P Mage, J Chauvergne, M Trojani
• The angiotensin-I converting enzyme (ACE) gene I/D polymorphism and ACE levels in Pima Indians. (1 April, 1996)

  C A Foy, L J McCormack, W C Knowler, J H Barrett, A Catto, P J Grant
• Mosaicism for the fragile X syndrome full mutation and deletions within the CGG repeat of the FMR1 gene. (1 April, 1996)

  M Milà, S Castellví-Bel, A Sánchez, C Lázaro, M Villa, X Estivill
• Clinical, enzymatic, and molecular characterisation of a Portuguese family with a chronic form of GM2-gangliosidosis B1 variant. (1 April, 1996)

  M G Ribeiro, T Sonin, R A Pinto, A Fontes, H Ribeiro, E Pinto, M M Palmeira, M C Sá Miranda
• "Pure" partial trisomy 4q25-qter owing to a de novo 4;22 translocation. (1 April, 1996)

  R V Mikelsaar, I W Lurie, T E Ilus
• Genetics in primary care. Report on workshop of EC Concerted Action on Genetics Services in Europe (CAGSE) in association with the Royal College of GP Spring Meeting, Blackpool, UK, 28 April 1995. (1 April, 1996)

  R Harris, H Harris
• Renal and urological tract malformations caused by a 22q11 deletion. (1 April, 1996)

  K Devriendt, A Swillen, J P Fryns, W Proesmans, M Gewillig
• Unstable mutation in incontinentia pigmenti? (1 April, 1996)

  E Hatchwell