The purpose of this project is to explore the natural history and mode
of inheritance, carrier detection and prenatal diagnosis of
immunodeficiency syndromes and to determine as precisely as possible
the cellular and molecular defect responsible for abnormal immune
responses.
No Sub Projects information available for 5M01RR000037-38 0310
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
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Outcomes
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No Outcomes available for 5M01RR000037-38 0310
Clinical Studies
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History
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Similar Projects
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