22q11.2 deletion syndrome overview: Difference between revisions
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{{22q11.2 deletion syndrome}} | {{22q11.2 deletion syndrome}} | ||
Revision as of 14:27, 11 July 2017
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22q11.2 deletion syndrome Microchapters |
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Differentiating 22q11.2 deletion syndrome from other Diseases |
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Diagnosis |
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Treatment |
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Case Studies |
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22q11.2 deletion syndrome overview On the Web |
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American Roentgen Ray Society Images of 22q11.2 deletion syndrome overview |
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Risk calculators and risk factors for 22q11.2 deletion syndrome overview |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor-In-Chief: Cafer Zorkun, M.D., Ph.D. [2]
Overview
22q11.2 deletion syndrome is a disorder caused by the deletion of a small piece of chromosome 22. The deletion occurs near the middle of the chromosome at a location designated q11.2.