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Paternal genetic variants and risk of obstructive heart defects: A parent-of-origin approach.
Patel, Jenil; Bircan, Emine; Tang, Xinyu; Orloff, Mohammed; Hobbs, Charlotte A; Browne, Marilyn L; Botto, Lorenzo D; Finnell, Richard H; Jenkins, Mary M; Olshan, Andrew; Romitti, Paul A; Shaw, Gary M; Werler, Martha M; Li, Jingyun; Nembhard, Wendy N.
Afiliación
  • Patel J; Department of Epidemiology, Fay W. Boozman College of Public Health, University of Arkansas for Medical Sciences, Little Rock, AR, United States of America.
  • Bircan E; Arkansas Center for Birth Defects Research and Prevention, Fay W. Boozman College of Public Health, University of Arkansas for Medical Sciences, Little Rock, AR, United States of America.
  • Tang X; Department of Epidemiology, Human Genetics and Environmental Sciences, The University of Texas Health Science Center at Houston (UTHealth) School of Public Health, Dallas, TX, United States of America.
  • Orloff M; Department of Epidemiology, Fay W. Boozman College of Public Health, University of Arkansas for Medical Sciences, Little Rock, AR, United States of America.
  • Hobbs CA; Arkansas Center for Birth Defects Research and Prevention, Fay W. Boozman College of Public Health, University of Arkansas for Medical Sciences, Little Rock, AR, United States of America.
  • Browne ML; Biostatistics Program, Department of Pediatrics, College of Medicine, University of Arkansas for Medical Sciences, Arkansas Children's Research Institute, Little Rock, AR, United States of America.
  • Botto LD; Department of Epidemiology, Fay W. Boozman College of Public Health, University of Arkansas for Medical Sciences, Little Rock, AR, United States of America.
  • Finnell RH; Arkansas Center for Birth Defects Research and Prevention, Fay W. Boozman College of Public Health, University of Arkansas for Medical Sciences, Little Rock, AR, United States of America.
  • Jenkins MM; Rady Children's Institute for Genomic Medicine, San Diego, CA, United States of America.
  • Olshan A; Birth Defects Research Section, New York State Department of Health, Albany, NY, United States of America.
  • Romitti PA; Department of Epidemiology and Biostatistics, School of Public Health, University at Albany, Rensselaer, NY, United States of America.
  • Shaw GM; Division of Medical Genetics, Department of Pediatrics, University of Utah, Salt Lake City, UT, United States of America.
  • Werler MM; Department of Molecular and Cellular Biology, Center for Precision Environmental Health, Baylor College of Medicine, Houston, TX, United States of America.
  • Li J; National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, GA, United States of America.
  • Nembhard WN; Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States of America.
PLoS Genet ; 17(3): e1009413, 2021 03.
Article en En | MEDLINE | ID: mdl-33684136
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Variación Genética / Predisposición Genética a la Enfermedad / Patrón de Herencia / Cardiopatías Congénitas Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: PLoS Genet Asunto de la revista: GENETICA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
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PubMed Links
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Variación Genética / Predisposición Genética a la Enfermedad / Patrón de Herencia / Cardiopatías Congénitas Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: PLoS Genet Asunto de la revista: GENETICA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos