Funded by an IRDiRC member =

Research projects

UNITED KINGDOM

Cambridgeshire
CAMBRIDGE

ISO - Investigation of Segmental Overgrowth

Addenbrooke's Hospital

University of Cambridge Metabolic Research Laboratories

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UNITED KINGDOM

West Midlands
BIRMINGHAM

Phenotyping of rare genetic overgrowth disorders (POD) study

Birmingham Women's NHS Foundation Trust

Regional Genetics Unit

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GERMANY

Baden-Württemberg
HEIDELBERG

Li-Fraumeni syndrome-cancer predisposition syndrome registry

Deutsches Krebsforschungszentrum

KITZ - Hopp-Kindertumorzentrum Heidelberg

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GERMANY

Niedersachsen
HANNOVER

Li-Fraumeni syndrome-cancer predisposition syndrome registry

Medizinische Hochschule Hannover

Klinik für Pädiatrische Hämatologie und Onkologie

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UNITED KINGDOM

Cambridgeshire
CAMBRIDGE

NIHR BioResource - Rare Disease: MPMT - Multiple primary malignant tumours

Addenbrooke's Hospital

Academic Department of Medical Genetics

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ITALY

CAMPANIA
NAPOLI

Telethon Undiagnosed Disease Program - Revised Proposal

Azienda Ospedaliera Universitaria - Seconda Università degli Studi di Napoli

Laboratorio di Genetica Medica

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SWITZERLAND

Suisse Alémanique
BASEL

Massively parallel sequencing for gene discovery in lethal fetal disorders

Universitätsspital Basel

Abteilung für Medizinische Genetik

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UNITED KINGDOM

Cambridgeshire
HINXTON

The Deciphering Developmental Disorders (the DDD study)

Wellcome Trust Sanger Institute

DECIPHER

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UNITED KINGDOM

Devon
EXETER

Exploring the Genetics of Renal Developmental Disease

Royal Devon and Exeter Hospital - Wonford site

Department of Urology

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Multicentric Research projects

UNITED KINGDOM
West Midlands
BIRMINGHAM
National Autozygosity Mapping Resource
Birmingham Women's NHS Foundation Trust
Medical and Molecular Genetics, Norton Court
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UNITED KINGDOM
West Midlands
BIRMINGHAM
National Autozygosity Mapping Resource
University of Birmingham
Department of Medical and Molecular Genetics
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CANADA
Colombie-Britannique
VANCOUVER
Maternal Infant Child and Youth Research Network (MICYRN)
University of British Columbia
Maternal Infant Child and Youth Research Network
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FRANCE
ILE-DE-FRANCE
ORSAY
CAMINEMS: Integrated Micro-Nano-Opto Fluidic systems for high-content diagnosis and studies of rare cancer cells
Institut Curie
Macromolécules et Microsystèmes en Biologie et en Medecine
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GERMANY
Sachsen-Anhalt
MAGDEBURG
International Clearinghouse for Birth Defects Monitoring Systems
Universitätsklinikum Magdeburg A.ö.R
MONZ - Fehlbildungsmonitoring Sachsen-Anhalt
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ITALY
LAZIO
ROMA
UnRareNet: a muticenter collaborative research network for the identification and study of rare undiagnosed patients (completed)
IRCCS Ospedale Pediatrico Bambino Gesù - SEDE GIANICOLO
Servizio Clinico di Consulenza Genetica
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