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Trial record 33 of 54 for:    "Acrocephalosyndactylia" OR "Apert syndrome" OR "Craniosynostoses"

Genetic Modifiers for 22q11.2 Syndrome (VCFS)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00916955
Recruitment Status : Unknown
Verified August 2010 by State University of New York - Upstate Medical University.
Recruitment status was:  Recruiting
First Posted : June 10, 2009
Last Update Posted : January 6, 2015
Albert Einstein College of Medicine
Information provided by:
State University of New York - Upstate Medical University

No Study Results Posted on for this Study
  Recruitment Status : Unknown
  Estimated Primary Completion Date : February 2015
  Estimated Study Completion Date : February 2015