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Related Studies
Genetic Analysis of Fraser Syndrome and Fryns Syndrome
This study has been completed.
Study NCT00032877   Information provided by National Institutes of Health Clinical Center (CC)
First Received: April 4, 2002   Last Updated: March 3, 2008   History of Changes
Related Studies can be found by searching for the Conditions, Interventions, and Sponsors found in this study:
Conditions listed in this trial
Fraser Syndrome
Fryns Syndrome
Chromosomal Abnormalities
Abnormalities, Multiple
Additional conditions recognized in this trial
Chromosome Aberrations
Chromosome Disorders
Congenital Abnormalities
Eye Abnormalities
Laryngostenosis
Syndactyly
Syndrome
More general conditions related to this trial
Bone Diseases
Bone Diseases, Developmental
Disease
Dysostoses
Eye Diseases
Genetic Diseases, Inborn
Laryngeal Diseases
Limb Deformities, Congenital
Musculoskeletal Abnormalities
Musculoskeletal Diseases
Otorhinolaryngologic Diseases
Pathologic Processes
Respiratory Tract Diseases
Synostosis
Sponsors listed in this trial
National Human Genome Research Institute (NHGRI)


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