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Perrault syndrome: further evidence for genetic heterogeneity
Authors:Emma M. Jenkinson  Jill Clayton-Smith  Sarju Mehta  Christopher Bennett  Willie Reardon  Andrew Green  Simon H. S. Pearce  Giuseppe De Michele  Gerard S. Conway  Deirdre Cilliers  Natalie Moreton  Julian R. E. Davis  Dorothy Trump  William G. Newman
Affiliation:1. Genetic Medicine, Manchester Academic Health Services Centre (MAHSC), St. Mary’s Hospital, University of Manchester, Manchester, M13 9WL, UK
3. East Anglian Medical Genetics Service, Addenbrookes Hospital, Cambridge, CB2 0QQ, UK
4. Yorkshire Regional Genetics Service, Ashley Wing, St James’s University Hospital, Leeds, LS9 7TF, UK
5. National Centre for Medical Genetics, Our Lady’s Hospital for Sick Children, Crumlin, Dublin 12, Ireland
6. School of Medicine and Medical Science, University College Dublin, Dublin, Ireland
10. Institute of Genetic Medicine, Newcastle University, International Centre for Life, Central Parkway, Newcastle upon Tyne, NE1 3BZ, UK
7. Department of Neurological Sciences, Federico II University, Via S. Pansini 5, 80131, Naples, Italy
8. Department of Endocrinology, University College London Hospitals, 250 Euston Road, London, NW1 2BU, UK
9. Oxford Regional Genetics Centre, Oxford Radcliffe Hospital NHS Trust, The Churchill Old Road, Headington, Oxford, OX3 7LJ, UK
2. Endocrinology and Diabetes Group, Manchester Academic Health Services Centre (MAHSC), St. Mary’s Hospital, University of Manchester, Manchester, M13 9WL, UK
Abstract:
Keywords:
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