Prematurity, ventricular septal defect and dysmorphisms are independent predictors of pathogenic copy number variants: a retrospective study on array-CGH results and phenotypical features of 293 children with neurodevelopmental disorders and/or multiple congenital anomalies
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1824-7288
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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online resource.
- Erschienen in
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Prematurity, ventricular septal defect and dysmorphisms are independent predictors of pathogenic copy number variants: a retrospective study on array-CGH results and phenotypical features of 293 children with neurodevelopmental disorders and/or multiple congenital anomalies ; volume:44 ; number:1 ; day:9 ; month:3 ; year:2018 ; pages:1-13 ; date:12.2018
The Italian journal of pediatrics ; 44, Heft 1 (9.3.2018), 1-13, 12.2018
- Urheber
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Maini, I.
- Beteiligte Personen und Organisationen
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Ivanovski, I.
Djuric, O.
Caraffi, S. G.
Errichiello, E.
Marinelli, M.
Franchi, F.
Bizzarri, V.
Rosato, S.
Pollazzon, M.
Gelmini, C.
Malacarne, M.
Fusco, C.
Gargano, G.
Bernasconi, S.
Zuffardi, O.
Garavelli, L.
SpringerLink (Online service)
- DOI
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10.1186/s13052-018-0467-z
- URN
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urn:nbn:de:1111-201805143541
- Rechteinformation
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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14.08.2025, 11:00 MESZ
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Beteiligte
- Maini, I.
- Ivanovski, I.
- Djuric, O.
- Caraffi, S. G.
- Errichiello, E.
- Marinelli, M.
- Franchi, F.
- Bizzarri, V.
- Rosato, S.
- Pollazzon, M.
- Gelmini, C.
- Malacarne, M.
- Fusco, C.
- Gargano, G.
- Bernasconi, S.
- Zuffardi, O.
- Garavelli, L.
- SpringerLink (Online service)
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