Pierpont syndrome: A collaborative study

Author:

Wright Emma M.M. Burkitt1,Suri Mohnish2,White Susan M.345,de Leeuw Nicole6,Silfhout Anneke T. Vulto‐van6,Stewart Fiona7,McKee Shane7,Mansour Sahar8,Connell Fiona C9,Chopra Maya10,Kirk Edwin P.10,Devriendt Koen11,Reardon Willie12,Brunner Han4,Donnai Dian1

Affiliation:

1. Genetic Medicine, Manchester Academic Health Science Centre, University of Manchester and Central Manchester University Hospitals NHS Foundation Trust. St Mary's Hospital, Manchester, UK

2. Clinical Genetics Service, Nottingham University Hospitals NHS Trust, Nottingham, UK

3. Genetic Health Services Victoria, Royal Children's Hospital, Parkville, Victoria, Australia

4. Department of Paediatrics, University of Melbourne, Melbourne, Victoria, Australia

5. Murdoch Childrens Research Institute, Royal Children's Hospital, Melbourne, Victoria, Australia

6. Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands

7. Medical Genetics, Belfast City Hospital, Belfast, UK

8. South West Thames Regional Genetics Service, St George's Hospital, London, UK

9. South East Thames Regional Genetics Service, Guy's Hospital, London, UK

10. Department of Medical Genetics, Sydney Children's Hospital, Randwick, New South Wales, Australia

11. Departement Menselijke Erfelijkheid, Katholieke Universiteit Leuven, Leuven, Belgium

12. Our Lady's Hospital for Sick Children, Crumlin, Dublin, Ireland

Publisher

Wiley

Subject

Genetics(clinical),Genetics

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