Failure to detect the 22q11.2 duplication syndrome rearrangement among patients with schizophrenia
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1744-9081
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
-
Failure to detect the 22q11.2 duplication syndrome rearrangement among patients with schizophrenia ; volume:4 ; number:1 ; day:19 ; month:2 ; year:2008 ; pages:1-5 ; date:12.2008
Behavioral and brain functions ; 4, Heft 1 (19.2.2008), 1-5, 12.2008
- Creator
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Brunet, Anna
Armengol, Lluís
Pelaez, Trini
Guillamat, Roser
Vallès, Vicenç
Gabau, Elisabeth
Estivill, Xavier
Guitart, Miriam
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/1744-9081-4-10
- URN
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urn:nbn:de:101:1-2021080709424248430589
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:57 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Brunet, Anna
- Armengol, Lluís
- Pelaez, Trini
- Guillamat, Roser
- Vallès, Vicenç
- Gabau, Elisabeth
- Estivill, Xavier
- Guitart, Miriam
- SpringerLink (Online service)
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Preliminary study of noninvasive prenatal screening for 22q11.2 deletion/duplication syndrome using multiplex dPCR assay
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Contribution of schizophrenia polygenic burden to longitudinal phenotypic variance in 22q11.2 deletion syndrome
Risk gene-set and pathways in 22q11.2 deletion-related schizophrenia: a genealogical molecular approach
How to diagnose the 22q11.2 deletion syndrome in patients with schizophrenia: a case report
Combination of conventional immunohistochemistry and qRT-PCR to detect ALK rearrangement
The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia
Characterization of the past and current duplication activities in the human 22q11.2 region
Exploring pathway interactions to detect molecular mechanisms of disease: 22q11.2 deletion syndrome
22q11.2 duplication syndrome: elevated rate of autism spectrum disorder and need for medical screening
A deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and review
Tandem Duplication and Random Loss for mitogenome rearrangement in Symphurus (Teleost: Pleuronectiformes)
Preliminary study of noninvasive prenatal screening for 22q11.2 deletion/duplication syndrome using multiplex dPCR assay
Erratum to: 22q11.2 duplication syndrome: elevated rate of autism spectrum disorder and need for medical screening
Contribution of schizophrenia polygenic burden to longitudinal phenotypic variance in 22q11.2 deletion syndrome
Risk gene-set and pathways in 22q11.2 deletion-related schizophrenia: a genealogical molecular approach
How to diagnose the 22q11.2 deletion syndrome in patients with schizophrenia: a case report
Combination of conventional immunohistochemistry and qRT-PCR to detect ALK rearrangement
The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia
Characterization of the past and current duplication activities in the human 22q11.2 region
Exploring pathway interactions to detect molecular mechanisms of disease: 22q11.2 deletion syndrome
22q11.2 duplication syndrome: elevated rate of autism spectrum disorder and need for medical screening
A deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and review
Tandem Duplication and Random Loss for mitogenome rearrangement in Symphurus (Teleost: Pleuronectiformes)
Preliminary study of noninvasive prenatal screening for 22q11.2 deletion/duplication syndrome using multiplex dPCR assay
Erratum to: 22q11.2 duplication syndrome: elevated rate of autism spectrum disorder and need for medical screening
Contribution of schizophrenia polygenic burden to longitudinal phenotypic variance in 22q11.2 deletion syndrome
Risk gene-set and pathways in 22q11.2 deletion-related schizophrenia: a genealogical molecular approach
How to diagnose the 22q11.2 deletion syndrome in patients with schizophrenia: a case report