A paradigmatic autistic phenotype associated with loss of PCDH11Y and NLGN4Y genes
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1755-8794
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
A paradigmatic autistic phenotype associated with loss of PCDH11Y and NLGN4Y genes ; volume:14 ; number:1 ; day:8 ; month:4 ; year:2021 ; pages:1-5 ; date:12.2021
BMC medical genomics ; 14, Heft 1 (8.4.2021), 1-5, 12.2021
- Urheber
-
Nardello, Rosaria
Antona, Vincenzo
Mangano, Giuseppe Donato
Salpietro, Vincenzo
Mangano, Salvatore
Fontana, Antonina
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
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10.1186/s12920-021-00934-x
- URN
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urn:nbn:de:101:1-2021053013314649146282
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:47 MESZ
Datenpartner
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Beteiligte
- Nardello, Rosaria
- Antona, Vincenzo
- Mangano, Giuseppe Donato
- Salpietro, Vincenzo
- Mangano, Salvatore
- Fontana, Antonina
- SpringerLink (Online service)
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