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Original article
Microdeletions in FMR2 may be a significant cause of premature ovarian failure

Authors

  • Anna Murray aWessex Regional Genetics Laboratory, Salisbury District Hospital, Salisbury, Wiltshire SP2 8BJ, UK, bHuman Genetics, Princess Anne Hospital, Coxford Road, Southampton SO16 5YA, UK, cCobbold Laboratories, Middlesex Hospital, Mortimer Street, London, UK PubMed articlesGoogle scholar articles
  • James Webb aWessex Regional Genetics Laboratory, Salisbury District Hospital, Salisbury, Wiltshire SP2 8BJ, UK, bHuman Genetics, Princess Anne Hospital, Coxford Road, Southampton SO16 5YA, UK, cCobbold Laboratories, Middlesex Hospital, Mortimer Street, London, UK PubMed articlesGoogle scholar articles
  • Nick Dennis aWessex Regional Genetics Laboratory, Salisbury District Hospital, Salisbury, Wiltshire SP2 8BJ, UK, bHuman Genetics, Princess Anne Hospital, Coxford Road, Southampton SO16 5YA, UK, cCobbold Laboratories, Middlesex Hospital, Mortimer Street, London, UK PubMed articlesGoogle scholar articles
  • Gerard Conway aWessex Regional Genetics Laboratory, Salisbury District Hospital, Salisbury, Wiltshire SP2 8BJ, UK, bHuman Genetics, Princess Anne Hospital, Coxford Road, Southampton SO16 5YA, UK, cCobbold Laboratories, Middlesex Hospital, Mortimer Street, London, UK PubMed articlesGoogle scholar articles
  • Newton Morton aWessex Regional Genetics Laboratory, Salisbury District Hospital, Salisbury, Wiltshire SP2 8BJ, UK, bHuman Genetics, Princess Anne Hospital, Coxford Road, Southampton SO16 5YA, UK, cCobbold Laboratories, Middlesex Hospital, Mortimer Street, London, UK PubMed articlesGoogle scholar articles
  1. Dr Murray.
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Citation

Murray A, Webb J, Dennis N, et al
Microdeletions in FMR2 may be a significant cause of premature ovarian failure
Journal of Medical Genetics 1999;36:767-770.

Publication history

  • Revised June 4, 1999
  • Accepted June 16, 1999
  • First published October 1, 1999.
Online issue publication 
April 27, 2016

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Journal of Medical Genetics