Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic Development
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1573-2592
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
-
online resource.
- Erschienen in
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Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic Development ; volume:43 ; number:2 ; day:17 ; month:1 ; year:2023 ; pages:247-270 ; date:2.2023
Journal of clinical immunology ; 43, Heft 2 (17.1.2023), 247-270, 2.2023
- Klassifikation
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Medizin, Gesundheit
- Urheber
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Mustillo, Peter J.
Sullivan, Kathleen E.
Chinn, Ivan K.
Notarangelo, Luigi D.
Haddad, Elie
Davies, E. Graham
de la Morena, Maria Teresa
Hartog, Nicholas
Yu, Joyce E.
Hernandez-Trujillo, Vivian P.
Ip, Winnie
Franco, Jose
Gambineri, Eleonora
Hickey, Scott E.
Varga, Elizabeth
Markert, M. Louise
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
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10.1007/s10875-022-01418-y
- URN
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urn:nbn:de:101:1-2023042922392488019624
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 11:04 MESZ
Datenpartner
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Beteiligte
- Mustillo, Peter J.
- Sullivan, Kathleen E.
- Chinn, Ivan K.
- Notarangelo, Luigi D.
- Haddad, Elie
- Davies, E. Graham
- de la Morena, Maria Teresa
- Hartog, Nicholas
- Yu, Joyce E.
- Hernandez-Trujillo, Vivian P.
- Ip, Winnie
- Franco, Jose
- Gambineri, Eleonora
- Hickey, Scott E.
- Varga, Elizabeth
- Markert, M. Louise
- SpringerLink (Online service)
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Correction to: Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic Development
Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome
Complement Activation in 22q11.2 Deletion Syndrome
Atypical development of the executive attention network in children with chromosome 22q11.2 deletion syndrome
Genotype-phenotype correlation in 22q11.2 deletion syndrome
A case report of T-box 1 mutation causing phenotypic features of chromosome 22q11.2 deletion syndrome
How might stress contribute to increased risk for schizophrenia in children with chromosome 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
Common and specific impairments in attention functioning in girls with chromosome 22q11.2 deletion, fragile X or Turner syndromes
Mapping the deletion endpoints in individuals with 22q11.2 Deletion Syndrome by droplet digital PCR
Correction to: Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic Development
Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome
Complement Activation in 22q11.2 Deletion Syndrome
Atypical development of the executive attention network in children with chromosome 22q11.2 deletion syndrome
Genotype-phenotype correlation in 22q11.2 deletion syndrome
A case report of T-box 1 mutation causing phenotypic features of chromosome 22q11.2 deletion syndrome
How might stress contribute to increased risk for schizophrenia in children with chromosome 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
Common and specific impairments in attention functioning in girls with chromosome 22q11.2 deletion, fragile X or Turner syndromes
Mapping the deletion endpoints in individuals with 22q11.2 Deletion Syndrome by droplet digital PCR
Correction to: Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic Development
Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome
Complement Activation in 22q11.2 Deletion Syndrome
Atypical development of the executive attention network in children with chromosome 22q11.2 deletion syndrome
Genotype-phenotype correlation in 22q11.2 deletion syndrome
A case report of T-box 1 mutation causing phenotypic features of chromosome 22q11.2 deletion syndrome
How might stress contribute to increased risk for schizophrenia in children with chromosome 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
Common and specific impairments in attention functioning in girls with chromosome 22q11.2 deletion, fragile X or Turner syndromes