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Clinical trial

Identification of the Molecular Bases of Syndromic Congenital Neutropenia With Development Anomalies

NCT02866162 is registered in ClinicalTrials.gov with Centre Hospitalier Universitaire Dijon as lead sponsor.

NCT NCT02866162
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Registry record

As filed in ClinicalTrials.gov.

Title
Identification of the Molecular Bases of Syndromic Congenital Neutropenia With Development Anomalies
Lead sponsor
Centre Hospitalier Universitaire Dijon
Phase
Observational
Overall status
Completed
Start date
September 30, 2013
Completion date
Not reported
Enrollment
25 (actual)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

congenital neutropenia