Investigation of the Genetic Aetiology of the Developmental Eye Defects - Microphthalmia, Anophthalmia and Coloboma

Documents from [12/1999] to [08/2004]

Identity Statement

HAEU Reference Code
ESF-1148
Original Reference Code
NW 96
Physical Medium

Paper

Reference Archivists

Mathevon, Valerie; Meyer, Ruth Ingeborg

Context

Access Level
Closed Document, Open Description
Closed Until
1 Jan 2027
Administrative and Biographical History

The Network was approved by the ESF Netwrok Group in May 2001 for a three-year period.
The Co-Chairmen were Dr. Harry Campbell, from University of Edinburgh Medical School, and Professor Veronica van Heyningen, from Edinburgh Western General Hospital

Content and Structure

Abstract

The Network focuses on three relatively rare but severe eye conditions: microphthalmia, anophthalmia and coloboma, analysing the genes involved in the development of these diseases.

The dossier contains:
First Proposal and research assessments; revised proposal and research assessments; correspondence on the establishment of the Network; list of Coordination Committee members; scientific report of the symposium funded by ESF and Wellcome Trust, held in Glasgow, on 14 Sep 1999.
Documents, report and correspondence concerning the first Coordination Committee meeting, held in Strasbourg, on 24-25 May 2002.
Documents, report and correspondence concerning the first workshop held in Sorrento on 17-28 March 2003.
Documents, report and correspondence concerning the second workshop held in Sorrento, on 29-30 March 2004.

Conditions of Access and Use

Languages

English, French

Type of Archival Materials

Textual

Allied Materials

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