Article Text

PDF

Screening of microdeletions of chromosome 20 in patients with Alagille syndrome.
  1. C Desmaze,
  2. J F Deleuze,
  3. A M Dutrillaux,
  4. G Thomas,
  5. M Hadchouel,
  6. A Aurias
  1. CNRS URA 620, Institut Curie, Paris, France.

    Abstract

    We report a cytogenetic and molecular study of a series of patients with Alagille syndrome. All 14 patients were studied with high resolution banding techniques and eight of them were also analysed with non-radioactive in situ hybridisation of the cosmid probe D20S6. Seven of these eight patients were also studied for allelic losses at the D20S6 locus. No microdeletion of chromosome 20 was found in this series.

    Statistics from Altmetric.com

    Request permissions

    If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.