Table of contents

Letters to the editor

• Incidence of germline hMLH1 andhMSH2 mutations (HNPCC patients) among newly diagnosed colorectal cancers in a Slovenian population

  (1 July, 2000)

  METKA RAVNIK-GLAVAČ, UROŠ POTOČNIK, DAMJAN GLAVAČ
• Does the survival motor neuron protein (SMN) interact with Bcl-2? (1 July, 2000)

  DANIEL D COOVERT, THANH T LE, GLENN E MORRIS, NGUYEN THI MAN, MARTINA KRALEWSKI, MICHAEL SENDTNER, ARTHUR H M BURGHES
• Novel mutations in the homogentisate- 1,2-dioxygenase gene identified in Slovak patients with alkaptonuria (1 July, 2000)

  A ZATKOVÁ, H POLÁKOVÁ, L MICUTKOVÁ, M ZVARÍK, V BOŠÁK, E FERÁKOVÁ, J MATUŠEK, V FERÁK, L KÁDASI
• Clinical and molecular correlates of somatic mosaicism in neurofibromatosis 2 (1 July, 2000)

  M E BASER, A J WALLACE, T STRACHAN, D G R EVANS
• Many ΔF508 heterozygote neonates with transient hypertrypsinaemia have a second, mild CFTRmutation

  (1 July, 2000)

  JIM BOYNE, STEVE EVANS, RODNEY J POLLITT, CHRISTOPHER J TAYLOR, ANN DALTON
• Further evidence for genetic heterogeneity of autosomal dominant disorders with accumulation of multiple deletions of mitochondrial DNA (1 July, 2000)

  GERT VAN GOETHEM, ANN LÖFGREN, JEAN-JACQUES MARTIN, CHRISTINE VAN BROECKHOVEN
• Liebenberg syndrome: brachydactyly with joint dysplasia (MIM 186550): a second family (1 July, 2000)

  G TIBERIO, M C DIGILIO, M GRAZIANI, F TESTA, A GIANNOTTI
• Prenatal detection of trisomy for the entire long arm of chromosome 7 (1 July, 2000)

  B V NDAH, JEFFREY A STEAD, LEO R BRANCAZIO, MARYBETH HUMMEL, SHARON L WENGER
• Cockayne syndrome associated with low CSF 5-hydroxyindole acetic acid levels (1 July, 2000)

  C J ELLAWAY, A DUGGINS, V S FUNG, J W EARL, R KAMATH, P G PARSONS, J A ANTONY, K N NORTH
• Unilateral lobar pulmonary agenesis in sibs (1 July, 2000)

  SIV FOKSTUEN, ALBERT SCHINZEL