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Dissection of partial 21q monosomy in different phenotypes: clinical and molecular characterization of five cases and review of the literature.
Errichiello, Edoardo; Novara, Francesca; Cremante, Anna; Verri, Annapia; Galli, Jessica; Fazzi, Elisa; Bellotti, Daniela; Losa, Laura; Cisternino, Mariangela; Zuffardi, Orsetta.
Affiliation
  • Errichiello E; Department of Molecular Medicine, University of Pavia, Via Forlanini 14, 27100 Pavia, Italy.
  • Novara F; Department of Molecular Medicine, University of Pavia, Via Forlanini 14, 27100 Pavia, Italy.
  • Cremante A; National Neurological Institute IRCCS C, Mondino, Pavia, Italy.
  • Verri A; National Neurological Institute IRCCS C, Mondino, Pavia, Italy.
  • Galli J; Mother-Child Department, Child Neurology and Psychiatry Unit, Spedali Civili, Brescia, Italy.
  • Fazzi E; Mother-Child Department, Child Neurology and Psychiatry Unit, Spedali Civili, Brescia, Italy.
  • Bellotti D; Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
  • Losa L; Department of Pediatrics, IRCCS Policlinico San Matteo, University of Pavia, Pavia, Italy.
  • Cisternino M; Department of Pediatrics, IRCCS Policlinico San Matteo, University of Pavia, Pavia, Italy.
  • Zuffardi O; Department of Molecular Medicine, University of Pavia, Via Forlanini 14, 27100 Pavia, Italy.
Mol Cytogenet ; 9(1): 21, 2016.
Article in En | MEDLINE | ID: mdl-27625702
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Mol Cytogenet Year: 2016 Document type: Article Affiliation country: Italy Country of publication: United kingdom
Fulltext
Add to My VHL
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Mol Cytogenet Year: 2016 Document type: Article Affiliation country: Italy Country of publication: United kingdom