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Understanding the genetic aetiology in patients with XY DSD.

Authors
  • Ahmed, S F1
  • Bashamboo, A
  • Lucas-Herald, A
  • McElreavey, K
  • 1 School of Medicine, University of Glasgow, Royal Hospital for Sick Children, Yorkhill, Glasgow, UK. [email protected]
Type
Published Article
Journal
British Medical Bulletin
Publisher
Oxford University Press
Publication Date
Jan 01, 2013
Volume
106
Pages
67–89
Identifiers
DOI: 10.1093/bmb/ldt008
PMID: 23529942
Source
Medline
Keywords
License
Unknown

Abstract

There is a need to understand and improve the clinical utility of genetic analysis in the clinical setting of the patient with a suspected DSD. This will be even more important when parallel gene sequencing identifies variations in multiple genes.

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