Study of Phenotype and Genotype Correlations in Patients With Contiguous Gene Deletion Syndromes - Related Studies

Study of Phenotype and Genotype Correlations in Patients With Contiguous Gene Deletion Syndromes

This study has been completed.

Study NCT00004351. Last updated on June 23, 2005. Information provided by Office of Rare Diseases (ORD)

Find Related Studies by Searching for the Conditions, Interventions, and Sponsors found in this study:


1	Conditions listed in this trial
		Williams Syndrome
		Angelman Syndrome
		Prader-Willi Syndrome
		Shprintzen Syndrome
		Smith-Magenis Syndrome
		DiGeorge Syndrome
		Chromosome Abnormalities

2	Additional conditions recognized in this trial
		Chromosome Aberrations
		Chromosome Deletion
		Chromosome Disorders
		Cleft Palate
		Congenital Abnormalities
		Heart Defects, Congenital
		Syndrome

3	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

4	Sponsors listed in this trial
		National Institute of Neurological Disorders and Stroke (NINDS)
		Baylor College of Medicine