Complement Activation in 22q11.2 Deletion Syndrome

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1573-2592

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Complement Activation in 22q11.2 Deletion Syndrome ; volume:40 ; number:3 ; day:9 ; month:3 ; year:2020 ; pages:515-523 ; date:4.2020
Journal of clinical immunology ; 40, Heft 3 (9.3.2020), 515-523, 4.2020

Creator: Grinde, Dina
Øverland, Torstein
Lima, Kari
Schjalm, Camilla
Mollnes, Tom Eirik
Abrahamsen, Tore G.

Contributor: SpringerLink (Online service)

DOI: 10.1007/s10875-020-00766-x

URN: urn:nbn:de:101:1-2020062501385808464689

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

Last update: 14.08.2025, 10:57 AM CEST

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Grinde, Dina
Øverland, Torstein
Lima, Kari
Schjalm, Camilla
Mollnes, Tom Eirik
Abrahamsen, Tore G.
SpringerLink (Online service)

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Complement Activation in 22q11.2 Deletion Syndrome

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Other Objects (12)

Genotype-phenotype correlation 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

Otologic and audiologic findings in 22q11.2 deletion syndrome

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

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

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

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

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

Genomic findings in patients with clinical suspicion of 22q11.2 deletion syndrome

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Otologic and audiologic findings in 22q11.2 deletion syndrome

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

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

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

Otologic and audiologic findings in 22q11.2 deletion syndrome

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

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