Table of contents

Original articles

• Applications of comparative genomic hybridisation in constitutional chromosome studies (1 July, 1999)

  Claire J Breen, Lynn Barton, Aiveen Carey, Adam Dunlop, Mary Glancy, Keara Hall, Anne Marie Hegarty, M Tariq Khokhar, Monica Power, Karen Ryan, Andrew J Green, Raymond L Stallings
• Analysis of germline CDKN1C (p57^KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation

  (1 July, 1999)

  Wayne W K Lam, Izuho Hatada, Sachiko Ohishi, Tsunehiro Mukai, Johanna A Joyce, Trevor R P Cole, Dian Donnai, Wolf Reik, Paul N Schofield, Eamonn R Maher
• CDKN1C expression in Beckwith-Wiedemann syndrome patients with allele imbalance (1 July, 1999)

  Elizabeth M Algar, Gillian J Deeble, Peter J Smith
• A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus (1 July, 1999)

  Guy Van Camp, Henricus Kunst, Kris Flothmann, Wyman McGuirt, Jan Wauters, Henri Marres, Margriet Verstreken, Irina N Bespalova, Margit Burmeister, Paul H Van de Heyning, Richard J H Smith, Patrick J Willems, Cor W R J Cremers, Marci M Lesperance
• Atypical haemochromatosis: phenotypic spectrum and β₂-microglobulin candidate gene analysis

  (1 July, 1999)

  Ann P Walker, Daniel F Wallace, Jason Partridge, Adrian B Bomford, James S Dooley
• Double heterozygosity for mutations in the β-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy (1 July, 1999)

  Pascale Richard, Richard Isnard, Lucie Carrier, Olivier Dubourg, Yves Donatien, Bénédicte Mathieu, Gisèle Bonne, Françoise Gary, Philippe Charron, Albert Hagege, Michel Komajda, Ketty Schwartz, Bernard Hainque
• The effect of CAT trinucleotide interruptions on the age at onset of spinocerebellar ataxia type 1 (SCA1) (1 July, 1999)

  Zenjiro Matsuyama, Yuishin Izumi, Masakuni Kameyama, Hideshi Kawakami, Shigenobu Nakamura
• Two male patients with ring Y: definition of an interval in Yq contributing to Turner syndrome (1 July, 1999)

  Maria Tzancheva, Radka Kaneva, Philip Kumanov, Gareth Williams, Chris Tyler-Smith
• Angelman syndrome resulting from UBE3A mutations in 14 patients from eight families: clinical manifestations and genetic counselling (1 July, 1999)

  Anne Moncla, Perrine Malzac, Marie-Odile Livet, Marie-Antoinette Voelckel, Josette Mancini, Jean Christophe Delaroziere, Nicole Philip, Jean-François Mattei