2 studies found for:    "Legius syndrome" [DISEASE] OR NCT00916903 [ID-NUMBER]
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"Legius syndrome" [DISEASE] OR NCT00916903 [ID-NUMBER] (2 records)
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Rank Status Study
1 Enrolling by invitation Genetic Disease Gene Identification
Conditions: Congenital Vertical Talus;   Familial Encephalopathy With Neuroserpin Inclusion Bodies;   Idiopathic Generalised Epilepsy;   Familial Dementia;   X-Linked Mental Retardation
2 Active, not recruiting Study of Disease Severity in Adults With Neurofibromatosis Type 1 (NF1)
Conditions: Neurofibromatosis Type I;   Legius Syndrome

Indicates status has not been verified in more than two years