Table of contents

Letters to the editor

• No evidence of germline PTEN mutations in familial prostate cancer

  (1 March, 2000)

  MATTHEW S FORREST, STEPHEN M EDWARDS, RIFAT A HAMOUDI, DAVID P DEARNALEY, AUDREY ARDEN-JONES, ANNA DOWE, ANNETTE MURKIN, JO KELLY, M DAWN TEARE, DOUGLAS F EASTON, MARGARET A KNOWLES, D TIMOTHY BISHOP, ROSALIND A EELES, THE CRC/BPG UK FAMILIAL PROSTATE CANCER STUDY COLLABORATORS, THE EC BIOMED FAMILIAL PROSTATE CANCER STUDY COLLABORATORS
• Mutation analysis of H19 andNAP1L4 (hNAP2) candidate genes and IGF2 DMR2 in Beckwith-Wiedemann syndrome

  (1 March, 2000)

  DANIEL CATCHPOOLE, ALAN V SMALLWOOD, JOHANNA A JOYCE, ADELE MURRELL, WAYNE LAM, TONGWEI TANG, DAVID MUNROE, WOLF REIK, PAUL N SCHOFIELD, EAMONN R MAHER
• A novel mutation in the CFTR gene correlates with severe clinical phenotype in seven Hispanic patients

  (1 March, 2000)

  JIANJUN WANG, MICHAEL C BOWMAN, EVELYN HSU, KARIN WERTZ, LEE-JUN C WONG
• The continuing failure to recognise Alström syndrome and further evidence of genetic homogeneity (1 March, 2000)

  VANESSA JAYNE DEEBLE, EMMA ROBERTS, ANDREW JACKSON, NICHOLAS LENCH, GULSHAN KARBANI, CHRISTOPHER GEOFFERY WOODS
• Clinical and radiographic features of a family with hypochondroplasia owing to a novel Asn540Ser mutation in the fibroblast growth factor receptor 3 gene (1 March, 2000)

  GEERT MORTIER, LIEVE NUYTINCK, MARGARITA CRAEN, JEAN-PIERRE RENARD, JULES G LEROY, ANNE DE PAEPE
• Screening British CADASIL families for mutations in theNOTCH3 gene

  (1 March, 2000)

  R P J DE LANGE, J BOLT, E REID, R DA SILVA, D J SHAW, D M ST CLAIR
• Correlation between mutations and age in cystic fibrosis in a French Canadian population (1 March, 2000)

  SYLVAIN R RIVARD, CHRISTIAN ALLARD, JEAN-PIERRE LEBLANC, MARCEL MILOT, GERVAIS AUBIN, FERNAND SIMARD, CLAUDE FÉREC, MARC DE BRAEKELEER
• The heritability of high myopia: a reanalysis of Goldschmidt's data (1 March, 2000)

  JEREMY A GUGGENHEIM, GEORGE KIROV, STUART A HODSON
• Progressive neurological deterioration in a child with distal arthrogryposis and whistling face (1 March, 2000)

  DORIT LEV, MIRIAM YANOOV, SHLOMO WEINTRAUB, TALLY LERMAN-SAGIE
• Chromosomal duplication of band 10p14 segregating through four generations (1 March, 2000)

  LUCILLE VOULLAIRE, R J MCKINLAY GARDNER, CATHRYN VAUX, ANNE ROBERTSON, RALPH OERTEL, HOWARD SLATER
• Somatic mosaicism associated with a mild Alport syndrome phenotype (1 March, 2000)

  KATE E PLANT, EILEEN BOYE, PETER M GREEN, DAVID VETRIE, FRANCES A FLINTER