Table of contents

Letters to JMG

• Rapid, high throughput prenatal detection of aneuploidy using a novel quantitative method (MLPA) (18 December, 2003)

  H R Slater, D L Bruno, H Ren, M Pertile, J P Schouten, K H A Choo
• A novel mutation in a patient with insulin-like growth factor 1 (IGF1) deficiency (18 December, 2003)

  G Bonapace, D Concolino, S Formicola, P Strisciuglio
• APOE and TGF-β1 genes are associated with obesity phenotypes (18 December, 2003)

  J-R Long, P-Y Liu, Y-J Liu, Y Lu, D-H Xiong, L Elze, R R Recker, H-W Deng
• Inbreeding and risk of late onset complex disease (18 December, 2003)

  I Rudan, D Rudan, H Campbell, A Carothers, A Wright, N Smolej-Narancic, B Janicijevic, L Jin, R Chakraborty, R Deka, P Rudan
• Association of single nucleotide polymorphisms in the oxidised LDL receptor 1 (OLR1) gene in patients with acute myocardial infarction (18 December, 2003)

  R Mango, F Clementi, P Borgiani, G B Forleo, M Federici, G Contino, E Giardina, L Garza, I E Fahdi, R Lauro, J L Mehta, G Novelli, F Romeo
• Congenital abnormalities reported in Pelger-Huët homozygosity as compared to Greenberg/HEM dysplasia: highly variable expression of allelic phenotypes (18 December, 2003)

  J C Oosterwijk, S Mansour, G van Noort, H R Waterham, C M Hall, R C M Hennekam
• A recurrent R718W mutation in COMP results in multiple epiphyseal dysplasia with mild myopathy: clinical and pathogenetic overlap with collagen IX mutations

  (18 December, 2003)

  E Jakkula, J Lohiniva, A Capone, L Bonafe, M Marti, V Schuster, A Giedion, G Eich, E Boltshauser, L Ala-Kokko, A Superti-Furga