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Replication of Genome Wide Association Identified Candidate Genes Confirm the Role of Common and Rare Variants in PAX7 and VAX1 in the Etiology of Nonsyndromic CL(P)
Authors:Azeez Butali  Satoshi Suzuki  Margaret E. Cooper  Adela M. Mansilla  Karen Cuenco  Elizabeth J. Leslie  Yasushi Suzuki  Teruyuki Niimi  Masahiko Yamamoto  Gongorjav Ayanga  Tudevdorj Erkhembaatar  Hiroo Furukawa  Kumiko Fujiwawa  Hideto Imura  Aline L. Petrin  Nagato Natsume  Terri H. Beaty  Mary L. Marazita  Jeffery C. Murray M.D.
Affiliation:1. Department of Pediatrics, University of Iowa, , Iowa City, Iowa;2. Division of Research and Treatment for Oral and Maxillofacial Congenital Anomalies, School of Dentistry, Aichi‐Gakuin University, , Japan;3. Faculty of Psychological and Physical Science, Aichi‐Gakuin University, , Japan;4. School of Public Health, Johns Hopkins University, , Baltimore, Maryland;5. Maternal and Children's Health Research Center Hospital, , Ulaanbaatar, Mongolia;6. Department of Oral Biology, School of Dental Medicine, Center for Craniofacial and Dental Genetics, University of Pittsburgh, , Pittsburgh, PA 15260;7. Department of Human Genetics, School of Public Health, University of Pittsburgh, , Pittsburgh, Pennsylvania;8. Departments of Pediatric Dentistry, Epidemiology, and Biology, University of Iowa, , Iowa City, Iowa;9. College of Nursing, University of Iowa, , Iowa City, Iowa
Abstract:
Keywords:GWAS  PAX7  VAX1  CL(P)
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