Viewing Study NCT01842659


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Study NCT ID: NCT01842659
Status: UNKNOWN
Last Update Posted: 2016-08-24
First Post: 2013-04-24
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Prenatal Screening for Imprinting Anomalies Implicated in Beckwith Wiedemann and Silver Russell Syndromes
Sponsor: Assistance Publique - Hôpitaux de Paris
Organization:

Study Modules

Identification Module Status Module Sponsor Collaborators Module Oversight Module Description Module Conditions Module Design Module Arms Interventions Module Outcomes Module Eligibility Module Contacts Locations Module