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Study of Phenotype and Genotype Correlations in Patients With Contiguous Gene Deletion Syndromes
This study has been completed.
Study NCT00004351 Information provided by Office of Rare Diseases (ORD)
First Received: October 18, 1999 Last Updated: June 23, 2005
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
Williams Syndrome
Angelman Syndrome
Prader-Willi Syndrome
Shprintzen Syndrome
Smith-Magenis Syndrome
DiGeorge Syndrome
Chromosome Abnormalities
Additional conditions recognized in this trial
Chromosome Aberrations
Chromosome Deletion
Chromosome Disorders
Cleft Palate
Congenital Abnormalities
Heart Defects, Congenital
Syndrome
More general conditions related to this trial
Abnormalities, Multiple
Aortic Stenosis, Supravalvular
Aortic Valve Stenosis
Cardiovascular Abnormalities
Cardiovascular Diseases
Central Nervous System Diseases
Craniofacial Abnormalities
Disease
Endocrine System Diseases
Genetic Diseases, Inborn
Heart Diseases
Heart Valve Diseases
Hypoparathyroidism
Immune System Diseases
Immunologic Deficiency Syndromes
Jaw Abnormalities
Jaw Diseases
Maxillofacial Abnormalities
Mental Retardation
Mouth Abnormalities
Mouth Diseases
Movement Disorders
Musculoskeletal Abnormalities
Musculoskeletal Diseases
Nervous System Diseases
Neurobehavioral Manifestations
Neurologic Manifestations
Nutrition Disorders
Obesity
Overnutrition
Parathyroid Diseases
Pathologic Processes
Stomatognathic Diseases
Stomatognathic System Abnormalities
Sponsors listed in this trial
National Institute of Neurological Disorders and Stroke (NINDS)
Baylor College of Medicine
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