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About the beta-thalassemia project by Stanley M. Diamond, Project Director For years, thalassemia, or Cooley's anemia, was thought to affect only Greek, Italian, Asian, and Sephardic Jewish families. In recent years, it became clear that Ashkenazic Jews also carry the trait and could be at risk for the fatal disease. In 1993, Dr. Charles Scriver (Montreal) and Dr. Ariella Oppenheim (Jerusalem) independently discovered that my family and a family in Jerusalem carry a newly identified mutation of this trait. As a result, I launched a project for which I need the participation of genealogists, the press, and the medical and scientific community around the world.
This research is being done in conjunction with the McGill University-Montreal Children's Hospital Medical Research Institute and Hebrew University-Hadassah Hospital, Department of Hematology, Jerusalem. The first medical paper on the project was published in the scientific journal Human Mutation 9:86-87 (January 1997).
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