Characterization of Three Overlapping Deletions Causing X-Linked Lymphoproliferative Disease Journal Articles uri icon

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abstract

  • Blot hybridization was used to find DNA sequences missing in a male who lacked two-thirds of Xq25. The probes were used to discover two additional males with deletions resulting in X-linked lymphoproliferative disease (XLP). All three deletions have a region in common, and DXS739 is within this candidate region. The new deletions were also detectable using chromosome banding, and the smallest removes only one-third of Xq25. XLP is the only consequence of the deletions.

authors

  • Skare, James
  • Wu, Bai-Lin
  • Madan, Suneeta
  • Pulijaal, Venkat
  • Purtilo, David
  • Haber, Daniel
  • Nelson, David
  • Sylla, Bakary
  • Grierson, Helen
  • Nitowsky, Harold
  • Glaser, Joy
  • Wissink, Julie
  • White, Bradley
  • Holden, Jeanette
  • Housman, David
  • Lenoir, Gilbert
  • Wyandt, Herman
  • Milunsky, Aubrey

publication date

  • April 1993