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The Beta-Thalassemia Project

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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.

"Mr. Diamond's work serves as a paradigm for the link between genealogy research and the study of the evolution and spread of genetic diseases."

 

Dr. Ariella Oppenheim, Professor of Experimental Hematology, Hebrew University-Hadassah Medical School, with Stanley M. Diamond.

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).

Dr. Charles Scriver and Stanley M. Diamond

 

"Genes and genealogy are different facets of a shared coin in personal history."

Dr. Charles R. Scriver, Alva Professor of Human Genetics, McGill University - Montreal Children's Hospital Research Institute, with Stanley M. Diamond.

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Copyright © 2002 - 2004 by Stanley M. Diamond.
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Date revised: August 03, 2004