Parental experiences and needs of caring for a child with 22q11.2 deletion syndrome

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: 1 Online-Ressource.

Language: Englisch

Bibliographic citation: Parental experiences and needs of caring for a child with 22q11.2 deletion syndrome ; volume:18 ; number:1 ; day:4 ; month:12 ; year:2023 ; pages:1-9 ; date:12.2023
Orphanet journal of rare diseases ; 18, Heft 1 (4.12.2023), 1-9, 12.2023

Creator: Walkowiak, Dariusz
Domaradzki, Jan

Contributor: SpringerLink (Online service)

DOI: 10.1186/s13023-023-02980-3

URN: urn:nbn:de:101:1-2024022011445846227333

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

Last update: 14.08.2025, 10:43 AM CEST

Data provider

This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.

Show original at data provider

Associated

Walkowiak, Dariusz
Domaradzki, Jan
SpringerLink (Online service)

Other Objects (12)

Complement Activation in 22q11.2 Deletion Syndrome

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

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

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

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

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

Social cognition in 22q11.2 deletion syndrome and idiopathic developmental neuropsychiatric disorders

Complement Activation in 22q11.2 Deletion Syndrome

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

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

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

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

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

Social cognition in 22q11.2 deletion syndrome and idiopathic developmental neuropsychiatric disorders

Complement Activation in 22q11.2 Deletion Syndrome

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

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

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

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

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

Social cognition in 22q11.2 deletion syndrome and idiopathic developmental neuropsychiatric disorders

Cultural heritage institutions wishing to register will find more information here.

Fields marked * need to be filled in.

Username*

Please enter your username

Email*

Please enter your email address

Please do not fill this field

First name

Last name

Password*

Please enter your password

Confirm password*

Please enter the same password

I have read the terms of use and the privacy policy for the collection of personal data and accept them. *

This field is required.

I would like to subscribe to the newsletter of the Deutsche Digitale Bibliothek. See newsletter subscription info.

Account created

Your "My DDB" account has been successfully created. Before you can log in to your account, you must click the confirmation link in the message we just sent to the email address you provided.

Parental experiences and needs of caring for a child with 22q11.2 deletion syndrome

Object Details

References and Relationships

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

Complement Activation in 22q11.2 Deletion Syndrome

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

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

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

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

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

Social cognition in 22q11.2 deletion syndrome and idiopathic developmental neuropsychiatric disorders

Complement Activation in 22q11.2 Deletion Syndrome

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

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

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

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

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

Social cognition in 22q11.2 deletion syndrome and idiopathic developmental neuropsychiatric disorders

Complement Activation in 22q11.2 Deletion Syndrome

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

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

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

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

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

Social cognition in 22q11.2 deletion syndrome and idiopathic developmental neuropsychiatric disorders

Related objects

Reset password