Inside the 8p23.1 duplication syndrome; eight microduplications of likely or uncertain clinical significance

Author:

Barber John C. K.1,Rosenfeld Jill A.2,Graham John M.3,Kramer Nancy3,Lachlan Katherine L.4,Bateman Mark S.5,Collinson Morag N.5,Stadheim Barbro Fossøy6,Turner Claire L. S.7,Gauthier Jacqueline N.8,Reimschisel Tyler E.8,Qureshi Athar M.9,Dabir Tabib A.10,Humphreys Mervyn W.11,Marble Michael12,Huang Taosheng13,Beal Sarah J.5,Massiah Joanne5,Taylor Emma-Jane5,Wynn Sarah L.14

Affiliation:

1. Department of Human Genetics and Genomic Medicine; University of Southampton; Southampton UK

2. Signature Genomic Laboratories; PerkinElmer Inc.; Spokane Washington

3. Medical Genetics Institute; Cedars Sinai Medical Center; Los Angeles California

4. Wessex Clinical Genetics Service; University Hospital Southampton NHS Foundation Trust; Southampton UK

5. Wessex Regional Genetics Laboratory; Salisbury NHS Foundation Trust; Salisbury UK

6. Department of Medical Genetics; Rikshospitalet; Oslo University Hospital; Oslo Norway

7. Department of Clinical Genetics; Royal Devon and Exeter Hospital (Heavitree); Exeter UK

8. Division of Developmental Medicine and the Centre for Child Development; Vanderbilt University Medical Center; Nashville Tennessee

9. Center for Pediatric and Congenital Heart Disease; The Cleveland Clinic; Cleveland Ohio

10. Medical Genetics Department; Belfast Health and Social Care Trust; Belfast City Hospital; Belfast Northern Ireland

11. Northern Ireland Regional Genetics Centre; Belfast Health and Social Care Trust; Belfast City Hospital; Belfast Northern Ireland

12. Children's Hospital of New Orleans; New Orleans Louisiana

13. School of Medicine; University of California; Irvine California

14. Unique; Caterham UK

Publisher

Wiley

Subject

Genetics(clinical),Genetics

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