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Array comparative genomic hybridisation analysis of boys with X-linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3
  1. Nicola M Solomon1,
  2. Shelley A Ross1,
  3. Susan M Forrest1,
  4. Paul Q Thomas1,
  5. Thomas Morgan2,
  6. Joseph L Belsky2,
  7. Frans A Hol3,
  8. Pamela S Karnes4,
  9. Nancy J Hopwood5,
  10. Susan E Myers6,
  11. Anjanette S Tan7,
  12. Garry L Warne8
  1. 1Murdoch Childrens Research Institute, Royal Children’s Hospital, Melbourne, Australia
  2. 2Yale University School of Medicine, Department of Genetics, New Haven, USA
  3. 3Department of Human Genetics, University Medical Center Nijmegen, The Netherlands
  4. 4Mayo Clinic, University of Medical Genetics, Rochester, Minnesota, USA
  5. 5University of Michigan Medical Center, Mississippi, USA
  6. 6Saint Louis University, Missouri, USA
  7. 7Division of Endocrinology, Diabetes, and Metabolism, University of Missouri-Columbia, Columbia, Missouri, USA
  8. 8Department of Endocrinology, Royal Children’s Hospital, Melbourne, Australia

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    In our previous article,1 we used array-comparative genomic hybridisation (CGH) analysis to identify Xq26–q27 duplications in families with X-linked hypopituitarism (XH). The array-CGH assay was validated using affected male genomic DNA from two previously characterised XH families that carry Xq26–q27 …

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