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Could a chimeric condition be responsible for unexpected genetic syndromes? The role of the single nucleotide polymorphism-array analysis.
Bottega, Roberta; Cappellani, Stefania; Fabretto, Antonella; Spinelli, Alessandro Mauro; Severini, Giovanni Maria; Aloisio, Michelangelo; Faleschini, Michela; Athanasakis, Emmanouil; Bruno, Irene; Faletra, Flavio; Pecile, Vanna.
Afiliación
  • Bottega R; Institute for Maternal and Child Health - IRCCS "Burlo Garofolo", Trieste, Italy.
  • Cappellani S; Institute for Maternal and Child Health - IRCCS "Burlo Garofolo", Trieste, Italy.
  • Fabretto A; Institute for Maternal and Child Health - IRCCS "Burlo Garofolo", Trieste, Italy.
  • Spinelli AM; University of Udine, Udine, Italy.
  • Severini GM; Institute for Maternal and Child Health - IRCCS "Burlo Garofolo", Trieste, Italy.
  • Aloisio M; Institute for Maternal and Child Health - IRCCS "Burlo Garofolo", Trieste, Italy.
  • Faleschini M; Institute for Maternal and Child Health - IRCCS "Burlo Garofolo", Trieste, Italy.
  • Athanasakis E; Institute for Maternal and Child Health - IRCCS "Burlo Garofolo", Trieste, Italy.
  • Bruno I; Institute for Maternal and Child Health - IRCCS "Burlo Garofolo", Trieste, Italy.
  • Faletra F; Institute for Maternal and Child Health - IRCCS "Burlo Garofolo", Trieste, Italy.
  • Pecile V; Institute for Maternal and Child Health - IRCCS "Burlo Garofolo", Trieste, Italy.
Mol Genet Genomic Med ; 7(3): e546, 2019 03.
Article en En | MEDLINE | ID: mdl-30628197
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Síndrome de Prader-Willi / Pruebas Genéticas / Polimorfismo de Nucleótido Simple / Quimerismo / Síndrome de Silver-Russell Tipo de estudio: Prognostic_studies Idioma: En Revista: Mol Genet Genomic Med Año: 2019 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Síndrome de Prader-Willi / Pruebas Genéticas / Polimorfismo de Nucleótido Simple / Quimerismo / Síndrome de Silver-Russell Tipo de estudio: Prognostic_studies Idioma: En Revista: Mol Genet Genomic Med Año: 2019 Tipo del documento: Article