Table of contents

Letters to the editor

• Sensitivity and predictive value of criteria for p53germline mutation screening

  (1 January, 2001)

  AGNÈS CHOMPRET, ANNE ABEL, DOMINIQUE STOPPA-LYONNET, LAURENCE BRUGIÈRES, SABINE PAGÈS, JEAN FEUNTEUN, CATHERINE BONAÏTI-PELLIÉ
• Identification of a transcriptionally compromised allele ofc-MYC in a North American family

  (1 January, 2001)

  DAVID SIWARSKI, JENNIFER KIM, LENA DIAW, KONRAD HUPPI
• E-cadherinis not frequently mutated in hereditary gastric cancer

  (1 January, 2001)

  EGLE AVIZIENYTE, VIRPI LAUNONEN, REIJO SALOVAARA, TUULA KIVILUOTO, LAURI A AALTONEN
• The spectrum and evolution of phenotypic findings in PTEN mutation positive cases of Bannayan-Riley-Ruvalcaba syndrome

  (1 January, 2001)

  MELISSA A PARISI, MARY BETH DINULOS, KATHLEEN A LEPPIG, VIRGINIA P SYBERT, CHARIS ENG, LOUANNE HUDGINS
• A frameshift mitochondrial complex I gene mutation in a patient with dystonia and cataracts: is the mutation pathogenic? (1 January, 2001)

  DAVID K SIMON, MARK A TARNOPOLSKY, J TIMOTHY GREENAMYRE, DONALD R JOHNS
• A common ancestor for COCH related cochleovestibular (DFNA9) patients in Belgium and The Netherlands bearing the P51S mutation

  (1 January, 2001)

  ERIK FRANSEN, MARGRIET VERSTREKEN, STEVEN J H BOM, FRANÇOIS LEMAIRE, MARTIJN H KEMPERMAN, YVETTE J M DE KOK, FLORIS L WUYTS, WIM I M VERHAGEN, PATRICK L M HUYGEN, WYMAN T MCGUIRT, RICHARD J H SMITH, LIONEL VAN MALDERGEM, FRANK DECLAU, COR W R J CREMERS, PAUL H VAN DE HEYNING, FRANS P M CREMERS, GUY VAN CAMP
• The spastic paraplegia SPG10 locus: narrowing of critical region and exclusion of sodium channel gene SCN8A as a candidate

  (1 January, 2001)

  E REID, A ESCAYG, A M DEARLOVE, D D LEE, M H MEISLER, D C RUBINSZTEIN
• Cytogenetic and molecular study of a jumping translocation in a baby with Dandy-Walker malformation (1 January, 2001)

  GENEVIÈVE LEFORT, PATRICIA BLANCHET, ANNE MARIE CHAZE, ANNE GIRARDET, PIERRE SARDA, JACQUES DEMAILLE, FRANCK PELLESTOR
• Clinical and cytogenetic characterisation of a patient with Down syndrome resulting from a 21q22.1→qter duplication (1 January, 2001)

  MARGA NADAL, CÉSAR GUZMÁN VIGO, MARIA ISABEL MELARAGNO, JOYCE A D ANDRADE, LUIS GARCIA ALONSO, DECIO BRUNONI, MELANIE PRITCHARD, XAVIER ESTIVILL
• Stable non-Robertsonian dicentric chromosomes: four new cases and a review (1 January, 2001)

  EMMANUELLE LEMYRE, VAZKEN M DER KALOUSTIAN, ALESSANDRA M V DUNCAN