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Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers.
Unolt, Marta; Versacci, Paolo; Anaclerio, Silvia; Lambiase, Caterina; Calcagni, Giulio; Trezzi, Matteo; Carotti, Adriano; Crowley, Terrence Blaine; Zackai, Elaine H; Goldmuntz, Elizabeth; Gaynor, James William; Digilio, Maria Cristina; McDonald-McGinn, Donna M; Marino, Bruno.
Afiliación
  • Unolt M; Department of Pediatrics and Pediatric Neuropsychiatry, "Sapienza" University of Rome, Rome, Italy.
  • Versacci P; Department of Pediatrics and Pediatric Neuropsychiatry, "Sapienza" University of Rome, Rome, Italy.
  • Anaclerio S; Department of Pediatrics and Pediatric Neuropsychiatry, "Sapienza" University of Rome, Rome, Italy.
  • Lambiase C; Department of Pediatrics and Pediatric Neuropsychiatry, "Sapienza" University of Rome, Rome, Italy.
  • Calcagni G; Department of Pediatric Cardiology and Cardiac Surgery, Bambino Gesù Pediatric Hospital, Rome, Italy.
  • Trezzi M; Department of Pediatric Cardiology and Cardiac Surgery, Bambino Gesù Pediatric Hospital, Rome, Italy.
  • Carotti A; Department of Pediatric Cardiology and Cardiac Surgery, Bambino Gesù Pediatric Hospital, Rome, Italy.
  • Crowley TB; Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Zackai EH; Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Goldmuntz E; The Cardiac Center, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Gaynor JW; The Cardiac Center, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Digilio MC; Division of Medical Genetics, Bambino Gesù Pediatric Hospital, Rome, Italy.
  • McDonald-McGinn DM; Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Marino B; Department of Pediatrics and Pediatric Neuropsychiatry, "Sapienza" University of Rome, Rome, Italy.
Am J Med Genet A ; 176(10): 2087-2098, 2018 10.
Article en En | MEDLINE | ID: mdl-29663641
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de DiGeorge / Cardiopatías Congénitas Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Pregnancy Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: Italia
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de DiGeorge / Cardiopatías Congénitas Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Pregnancy Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: Italia