Erratum to: 22q11.2 duplication syndrome: elevated rate of autism spectrum disorder and need for medical screening

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 2040-2392

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: 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

Creator: Wenger, Tara L.

Contributor: 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

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:22 AM CEST

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Associated

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)

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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

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Juveniler Parkinson und Mikrodeletionssyndrom 22q11.2

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Erratum to: 22q11.2 duplication syndrome: elevated rate of autism spectrum disorder and need for medical screening

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Other Objects (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

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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

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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?

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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

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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?

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