Table of contents

Letters to JMG

• Characterisation of the growth regulating gene IMP3, a candidate for Silver-Russell syndrome

  (1 August, 2002)

  D Monk, L Bentley, C Beechey, M Hitchins, J Peters, M A Preece, P Stanier, G E Moore
• Silver-Russell phenotype in a patient with pure trisomy 1q32.1-q42.1: further delineation of the pure 1q trisomy syndrome (1 August, 2002)

  M M van Haelst, H J F M M Eussen, F Visscher, J L M de Ruijter, S L S Drop, D Lindhout, C H Wouters, L C P Govaerts
• MECP2 gene nucleotide changes and their pathogenicity in males: proceed with caution

  (1 August, 2002)

  F Laccone, B Zoll, P Huppke, F Hanefeld, W Pepinski, R Trappe
• Twelve novel FBN1 mutations in Marfan syndrome and Marfan related phenotypes test the feasibility of FBN1 mutation testing in clinical practice

  (1 August, 2002)

  D J Halliday, S Hutchinson, L Lonie, J A Hurst, H Firth, P A Handford, P Wordsworth
• Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype

  (1 August, 2002)

  L Faivre, V Cormier-Daire, J M Lapierre, L Colleaux, S Jacquemont, D Geneviéve, P Saunier, A Munnich, C Turleau, S Romana, M Prieur, M C De Blois, M Vekemans
• The phenotype of survivors of campomelic dysplasia (1 August, 2002)

  S Mansour, A C Offiah, S McDowall, P Sim, J Tolmie, C Hall
• Dysosteosclerosis: a report of three new cases and evolution of the radiological findings (1 August, 2002)

  N H Elçioglu, A Vellodi, C M Hall
• A significant response to neoadjuvant chemotherapy in BRCA1/2 related breast cancer

  (1 August, 2002)

  P O Chappuis, J Goffin, N Wong, C Perret, P Ghadirian, P N Tonin, W D Foulkes
• Incidence of non-founder BRCA1 and BRCA2 mutations in high risk Ashkenazi breast and ovarian cancer families

  (1 August, 2002)

  N D Kauff, P Perez-Segura, M E Robson, L Scheuer, B Siegel, A Schluger, B Rapaport, T S Frank, K Nafa, N A Ellis, G Parmigiani, K Offit