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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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1755-8166

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Co-existence of other copy number variations with 22q11.2 deletion or duplication: a modifier for variable phenotypes of the syndrome? ; volume:5 ; number:1 ; day:9 ; month:4 ; year:2012 ; pages:1-4 ; date:12.2012
Molecular cytogenetics ; 5, Heft 1 (9.4.2012), 1-4, 12.2012

Creator: Li, Deling
Tekin, Mustafa
Buch, Maria
Fan, Yao-Shan

Contributor: SpringerLink (Online service)

DOI: 10.1186/1755-8166-5-18

URN: urn:nbn:de:101:1-2021082520402396765151

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 11:02 AM CEST

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Li, Deling
Tekin, Mustafa
Buch, Maria
Fan, Yao-Shan
SpringerLink (Online service)

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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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Other Objects (12)

A deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and review

Complement Activation in 22q11.2 Deletion Syndrome

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Genotype-phenotype correlation in 22q11.2 deletion syndrome

Otologic and audiologic findings in 22q11.2 deletion syndrome

Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome

Developmental trajectories of executive functions in 22q11.2 deletion syndrome

Mapping the deletion endpoints in individuals with 22q11.2 Deletion Syndrome by droplet digital PCR

Intergenerational and intrafamilial phenotypic variability in 22q11.2 Deletion syndrome subjects

Neural correlates of socio-emotional perception in 22q11.2 deletion syndrome

Abnormal development of early auditory processing in 22q11.2 Deletion Syndrome

Failure to detect the 22q11.2 duplication syndrome rearrangement among patients with schizophrenia

A deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and review

Complement Activation in 22q11.2 Deletion Syndrome

Preliminary study of noninvasive prenatal screening for 22q11.2 deletion/duplication syndrome using multiplex dPCR assay

Genotype-phenotype correlation in 22q11.2 deletion syndrome

Otologic and audiologic findings in 22q11.2 deletion syndrome

Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome

Developmental trajectories of executive functions in 22q11.2 deletion syndrome

Mapping the deletion endpoints in individuals with 22q11.2 Deletion Syndrome by droplet digital PCR

Intergenerational and intrafamilial phenotypic variability in 22q11.2 Deletion syndrome subjects

Neural correlates of socio-emotional perception in 22q11.2 deletion syndrome

Abnormal development of early auditory processing in 22q11.2 Deletion Syndrome

Failure to detect the 22q11.2 duplication syndrome rearrangement among patients with schizophrenia

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Complement Activation in 22q11.2 Deletion Syndrome

Preliminary study of noninvasive prenatal screening for 22q11.2 deletion/duplication syndrome using multiplex dPCR assay

Genotype-phenotype correlation in 22q11.2 deletion syndrome

Otologic and audiologic findings in 22q11.2 deletion syndrome

Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome

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Mapping the deletion endpoints in individuals with 22q11.2 Deletion Syndrome by droplet digital PCR

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Neural correlates of socio-emotional perception in 22q11.2 deletion syndrome

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Failure to detect the 22q11.2 duplication syndrome rearrangement among patients with schizophrenia

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