Genetic Analysis of Fraser Syndrome and Fryns Syndrome - Related Studies

Genetic Analysis of Fraser Syndrome and Fryns Syndrome

This study has been completed.

Study NCT00032877. Last updated on March 3, 2008. Information provided by National Institutes of Health Clinical Center (CC)

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1	Conditions listed in this trial
		Fraser Syndrome
		Fryns Syndrome
		Chromosomal Abnormalities
		Abnormalities, Multiple

2	Additional conditions recognized in this trial
		Chromosome Aberrations
		Chromosome Disorders
		Congenital Abnormalities
		Eye Abnormalities
		Laryngostenosis
		Syndactyly
		Syndrome

3	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

4	Sponsors listed in this trial
		National Human Genome Research Institute (NHGRI)