CompletedNot applicableNCT02885090
New Genes Involved in Molecular Etiology of Rett Syndrome Through DNA Microarray Comparative Genomic Hybridization
Studying Rett syndrome
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Central Hospital, Nancy, France
- Principal Investigator
- Christophe PHILIPPE,Laboratoire de Génétique Médicale, Rue du Morvan, 54511 Vandoeuvre-Les-Nancy Cédex
- Intervention
- Blood sampling(procedure)
- Enrollment
- 17 enrolled
- Eligibility
- All sexes
- Timeline
- 2010 – 2011
Study locations (9)
- Handicaps de l'Enfant - Pavillon Ste Marie, CHU St Jacques, Besançon, France
- Service de Neuropédiatrie, Hôpital St Jacques, CHU de Besançon, Besançon, France
- Unité de génétique, Groupe hospitalier Hôpital Flaubert, Caen, France
- Centre de Génétique Hôpital d'Enfants, CHU de Dijon, Dijon, France
- Service de neuropédiatrie, CHU Hôpital Gui de Chauliac, Montpellier, France
- Laboratoire de Génétique chromosomique, CHU Hôpital l'Archet 2, Nice, France
- Service de génétique médicale, CHU Hôpital Purpan, Nice, France
- Service de génétique médicale, CHU Hôpital Purpan, CHU de Toulouse, Toulouse, France
- Laboratoire de Génétique, Hôpitaux de Brabois, CHU de Nancy, Vandœuvre-lès-Nancy, France
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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