Erratum to: 22q11.2 duplication syndrome: elevated rate of autism spectrum disorder and need for medical screening
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
2040-2392
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Erratum to: 22q11.2 duplication syndrome: elevated rate of autism spectrum disorder and need for medical screening ; volume:7 ; number:1 ; day:13 ; month:7 ; year:2016 ; pages:1-2 ; date:12.2016
Molecular autism ; 7, Heft 1 (13.7.2016), 1-2, 12.2016
- Urheber
-
Wenger, Tara L.
- Beteiligte Personen und Organisationen
-
Miller, Judith S.
DePolo, Lauren M.
de Marchena, Ashley B.
Clements, Caitlin C.
Emanuel, Beverly S.
Zackai, Elaine H.
McDonald-McGinn, Donna M.
Schultz, Robert T.
SpringerLink (Online service)
- DOI
-
10.1186/s13229-016-0097-5
- URN
-
urn:nbn:de:101:1-2018071222392900916437
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:22 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Wenger, Tara L.
- Miller, Judith S.
- DePolo, Lauren M.
- de Marchena, Ashley B.
- Clements, Caitlin C.
- Emanuel, Beverly S.
- Zackai, Elaine H.
- McDonald-McGinn, Donna M.
- Schultz, Robert T.
- SpringerLink (Online service)
Ähnliche Objekte (12)
22q11.2 duplication syndrome: elevated rate of autism spectrum disorder and need for medical screening
Failure to detect the 22q11.2 duplication syndrome rearrangement among patients with schizophrenia
Characterization of the past and current duplication activities in the human 22q11.2 region
A deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and review
Critical region within 22q11.2 linked to higher rate of autism spectrum disorder
Preliminary study of noninvasive prenatal screening for 22q11.2 deletion/duplication syndrome using multiplex dPCR assay
Neuroanatomical underpinnings of autism symptomatology in carriers and non-carriers of the 22q11.2 microdeletion
Angstgeneralisierung bei Deletionssyndrom 22q11.2
A genetics-first approach to understanding autism and schizophrenia spectrum disorders: the 22q11.2 deletion syndrome
Erratum to: Glomerulopathy in patients with distal duplication of chromosome 6p
Juveniler Parkinson und Mikrodeletionssyndrom 22q11.2
Co-existence of other copy number variations with 22q11.2 deletion or duplication: a modifier for variable phenotypes of the syndrome?
22q11.2 duplication syndrome: elevated rate of autism spectrum disorder and need for medical screening
Failure to detect the 22q11.2 duplication syndrome rearrangement among patients with schizophrenia
Characterization of the past and current duplication activities in the human 22q11.2 region
A deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and review
Critical region within 22q11.2 linked to higher rate of autism spectrum disorder
Preliminary study of noninvasive prenatal screening for 22q11.2 deletion/duplication syndrome using multiplex dPCR assay
Neuroanatomical underpinnings of autism symptomatology in carriers and non-carriers of the 22q11.2 microdeletion
Angstgeneralisierung bei Deletionssyndrom 22q11.2
A genetics-first approach to understanding autism and schizophrenia spectrum disorders: the 22q11.2 deletion syndrome
Erratum to: Glomerulopathy in patients with distal duplication of chromosome 6p
Juveniler Parkinson und Mikrodeletionssyndrom 22q11.2
Co-existence of other copy number variations with 22q11.2 deletion or duplication: a modifier for variable phenotypes of the syndrome?
22q11.2 duplication syndrome: elevated rate of autism spectrum disorder and need for medical screening
Failure to detect the 22q11.2 duplication syndrome rearrangement among patients with schizophrenia
Characterization of the past and current duplication activities in the human 22q11.2 region
A deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and review
Critical region within 22q11.2 linked to higher rate of autism spectrum disorder
Preliminary study of noninvasive prenatal screening for 22q11.2 deletion/duplication syndrome using multiplex dPCR assay
Neuroanatomical underpinnings of autism symptomatology in carriers and non-carriers of the 22q11.2 microdeletion
Angstgeneralisierung bei Deletionssyndrom 22q11.2
A genetics-first approach to understanding autism and schizophrenia spectrum disorders: the 22q11.2 deletion syndrome
Erratum to: Glomerulopathy in patients with distal duplication of chromosome 6p
Juveniler Parkinson und Mikrodeletionssyndrom 22q11.2