Whole exome association of rare deletions in multiplex oral cleft families

Author:

Fu Jack1,Beaty Terri H.2,Scott Alan F.34,Hetmanski Jacqueline2,Parker Margaret M.5,Wilson Joan E. Bailey6,Marazita Mary L.7,Mangold Elisabeth8,Albacha-Hejazi Hasan9,Murray Jeffrey C.10,Bureau Alexandre11,Carey Jacob2,Cristiano Stephen1,Ruczinski Ingo1,Scharpf Robert B.12

Affiliation:

1. Department of Biostatistics; Johns Hopkins Bloomberg School of Public Health; Baltimore MD USA

2. Department of Epidemiology; Johns Hopkins Bloomberg School of Public Health; Baltimore MD USA

3. Center for Inherited Disease Research; Johns Hopkins School of Medicine; Baltimore MD USA

4. Institute of Genetic Medicine; Johns Hopkins School of Medicine; Baltimore MD USA

5. Channing Division of Network Medicine; Department of Medicine, Brigham and Women's Hospital; Boston MA USA

6. Inherited Disease Research Branch; National Human Genome Research Institute; National Institutes of Health; Baltimore MD USA

7. Department of Oral Biology; Center for Craniofacial and Dental Genetics; School of Dental Medicine, University of Pittsburgh; PA USA

8. Institute of Human Genetics; University of Bonn; Bonn Germany

9. Dr. Hejazi Clinic; Damascus Syrian Arab Republic

10. Department of Pediatrics; School of Medicine, University of Iowa; IA USA

11. Centre de Recherche de l'Institut Universitaire en Santé Mentale de Québec and Département de Médecine Sociale et Préventive; Université Laval; Québec Canada

12. Department of Oncology; Johns Hopkins School of Medicine; Baltimore MD USA

Funder

National Human Genome Research Institute

National Institutes of Health

Publisher

Wiley

Subject

Genetics(clinical),Epidemiology

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