Association studies of low-frequency coding variants in nonsyndromic cleft lip with or without cleft palate.
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| Title: | Association studies of low-frequency coding variants in nonsyndromic cleft lip with or without cleft palate. |
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| Authors: | Leslie EJ; Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania., Carlson JC; Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania., Shaffer JR; Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania., Buxó CJ; School of Dental Medicine, University of Puerto Rico, San Juan, Puerto Rico., Castilla EE; CEMIC: Center for Medical Education and Clinical Research, Buenos Aires, Argentina.; ECLAMC (Latin American Collaborative Study of Congenital Malformations) at INAGEMP (National Institute of Population Medical Genetics), Rio de Janeiro, Brazil.; Laboratory of Congenital Malformation Epidemiology, Oswaldo Cruz Institute, FIOCRUZ, Rio de Janeiro, Brazil., Christensen K; Department of Epidemiology, Institute of Public Health, University of Southern Denmark, Odense, Denmark., Deleyiannis FWB; Department of Surgery, Plastic and Reconstructive Surgery, University of Colorado School of Medicine, Denver, Colorado., Field LL; Department of Medical Genetics, University of British Columbia, Vancouver, Canada., Hecht JT; Department of Pediatrics, McGovern Medical School and School of Dentistry UT Health at Houston, Houston, Texas., Moreno L; Department of Orthodontics, College of Dentistry, University of Iowa, Iowa City, Iowa., Orioli IM; ECLAMC (Latin American Collaborative Study of Congenital Malformations) at INAGEMP (National Institute of Population Medical Genetics), Rio de Janeiro, Brazil.; Department of Genetics, Institute of Biology, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil., Padilla C; Department of Pediatrics, College of Medicine; and Institute of Human Genetics, National Institutes of Health, University of the Philippines Manila, Manila, The Philippines.; Philippine Genome Center, University of the Philippines System, Manila, The Philippines., Vieira AR; Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania., Wehby GL; Department of Health Management and Policy, College of Public Health, University of Iowa, Iowa City, Iowa., Feingold E; Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania., Weinberg SM; Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania., Murray JC; Department of Pediatrics, Carver College of Medicine, University of Iowa, Iowa City, Iowa., Marazita ML; Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.; Clinical and Translational Science, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania. |
| Source: | American journal of medical genetics. Part A [Am J Med Genet A] 2017 Jun; Vol. 173 (6), pp. 1531-1538. Date of Electronic Publication: 2017 Apr 19. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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