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Copy number variants in a population-based investigation of Klippel-Trenaunay syndrome.
Dimopoulos, Aggeliki; Sicko, Robert J; Kay, Denise M; Rigler, Shannon L; Fan, Ruzong; Romitti, Paul A; Browne, Marilyn L; Druschel, Charlotte M; Caggana, Michele; Brody, Lawrence C; Mills, James L.
Afiliación
  • Dimopoulos A; Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland.
  • Sicko RJ; Division of Genetics, Wadsworth Center, New York State Department of Health, Albany, New York.
  • Kay DM; Division of Genetics, Wadsworth Center, New York State Department of Health, Albany, New York.
  • Rigler SL; Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland.
  • Fan R; Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland.
  • Romitti PA; Department of Epidemiology, College of Public Health, The University of Iowa, Iowa City, Iowa.
  • Browne ML; Congenital Malformations Registry, New York State Department of Health, Albany, New York.
  • Druschel CM; Department of Epidemiology and Biostatistics, University at Albany School of Public Health, Rensselaer, New York.
  • Caggana M; Congenital Malformations Registry, New York State Department of Health, Albany, New York.
  • Brody LC; Department of Epidemiology and Biostatistics, University at Albany School of Public Health, Rensselaer, New York.
  • Mills JL; Division of Genetics, Wadsworth Center, New York State Department of Health, Albany, New York.
Am J Med Genet A ; 173(2): 352-359, 2017 Feb.
Article en En | MEDLINE | ID: mdl-27901321
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome de Klippel-Trenaunay-Weber / Estudios de Asociación Genética / Variaciones en el Número de Copia de ADN Tipo de estudio: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Humans Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2017 Tipo del documento: Article
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome de Klippel-Trenaunay-Weber / Estudios de Asociación Genética / Variaciones en el Número de Copia de ADN Tipo de estudio: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Humans Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2017 Tipo del documento: Article