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Association of low-frequency genetic variants in regulatory regions with nonsyndromic orofacial clefts.
Shaffer, John R; LeClair, Jessica; Carlson, Jenna C; Feingold, Eleanor; Buxó, Carmen J; Christensen, Kaare; Deleyiannis, Frederic W B; Field, L Leigh; Hecht, Jacqueline T; Moreno, Lina; Orioli, Ieda M; Padilla, Carmencita; Vieira, Alexandre R; Wehby, George L; Murray, Jeffrey C; Weinberg, Seth M; Marazita, Mary L; Leslie, Elizabeth J.
Afiliação
  • Shaffer JR; Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • LeClair J; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Carlson JC; Department of Computational and Systems Biology, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Feingold E; Department of Biostatistics, School of Public Health, Boston University, Boston, Massachusetts.
  • Buxó CJ; Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Christensen K; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Deleyiannis FWB; Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Field LL; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Hecht JT; Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Moreno L; Dental and Craniofacial Genomics Core, School of Dental Medicine, University of Puerto Rico, San Juan, Puerto Rico.
  • Orioli IM; Department of Epidemiology, Institute of Public Health, University of Southern Denmark, Odense, Denmark.
  • Padilla C; Department of Surgery, Plastic and Reconstructive Surgery, University of Colorado School of Medicine, Denver, Colorado.
  • Vieira AR; Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
  • Wehby GL; Department of Pediatrics, McGovern Medical School and School of Dentistry UT Health at Houston, Houston, Texas.
  • Murray JC; Department of Orthodontics, College of Dentistry, University of Iowa, Iowa City, Iowa.
  • Weinberg SM; Department of Genetics, Institute of Biology, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
  • Marazita ML; ECLAMC (Latin American Collaborative Study of Congenital Malformations) at INAGEMP (National Institute of Population Medical Genetics), Rio de Janeiro, Brazil.
  • Leslie EJ; Department of Pediatrics, College of Medicine; and Institute of Human Genetics, National Institutes of Health, University of the Philippines Manila, Manila, The Philippines.
Am J Med Genet A ; 179(3): 467-474, 2019 03.
Article em En | MEDLINE | ID: mdl-30582786
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / Encéfalo / Sequências Reguladoras de Ácido Nucleico / Fenda Labial / Fissura Palatina / Predisposição Genética para Doença / Estudos de Associação Genética Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / Encéfalo / Sequências Reguladoras de Ácido Nucleico / Fenda Labial / Fissura Palatina / Predisposição Genética para Doença / Estudos de Associação Genética Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article