Cargando…

Erratum to: 22q11.2 duplication syndrome: elevated rate of autism spectrum disorder and need for medical screening

Detalles Bibliográficos
Autores principales:	Wenger, Tara L., Miller, Judith S., DePolo, Lauren M., de Marchena, Ashley B., Clements, Caitlin C., Emanuel, Beverly S., Zackai, Elaine H., McDonald-McGinn, Donna M., Schultz, Robert T.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2016
Materias:	Erratum
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4944480/ https://www.ncbi.nlm.nih.gov/pubmed/27418956 http://dx.doi.org/10.1186/s13229-016-0097-5

Ejemplares similares

22q11.2 duplication syndrome: elevated rate of autism spectrum disorder and need for medical screening
por: Wenger, Tara L., et al.
Publicado: (2016)

Critical region within 22q11.2 linked to higher rate of autism spectrum disorder
por: Clements, Caitlin C., et al.
Publicado: (2017)

A Novel Non-Allelic Homologous Recombination Event in a Parent with an 11;22 Reciprocal Translocation Leading to 22q11.2 Deletion Syndrome
por: Pastor, Steven, et al.
Publicado: (2022)

22q11.2 Deletion and Duplication Syndromes and COVID-19
por: Crowley, T. Blaine, et al.
Publicado: (2022)

Influence of Parent-of-Origin on Intellectual Outcomes in the Chromosome 22q11.2 Deletion Syndrome
por: McGinn, Daniel E., et al.
Publicado: (2022)

Relationship between intelligence quotient measures and computerized neurocognitive performance in 22q11.2 deletion syndrome
por: Gur, Ruben C., et al.
Publicado: (2021)

Disrupted anatomic networks in the 22q11.2 deletion syndrome
por: Schmitt, J. Eric, et al.
Publicado: (2016)

The Role of mGluR Copy Number Variation in Genetic and Environmental Forms of Syndromic Autism Spectrum Disorder
por: Wenger, Tara L., et al.
Publicado: (2016)

Psychosis spectrum features, neurocognition and functioning in a longitudinal study of youth with 22q11.2 deletion syndrome
por: Gur, Raquel E., et al.
Publicado: (2023)

Pediatric healthcare costs for patients with 22q11.2 deletion syndrome
por: Benn, Peter, et al.
Publicado: (2017)

Pathogenic variants in CDC45 on the remaining allele in patients with a chromosome 22q11.2 deletion result in a novel autosomal recessive condition
por: Unolt, Marta, et al.
Publicado: (2019)

Coexisting Conditions Modifying Phenotypes of Patients with 22q11.2 Deletion Syndrome
por: Smyk, Marta, et al.
Publicado: (2023)

Optical mapping of the 22q11.2DS region reveals complex repeat structures and preferred locations for non-allelic homologous recombination (NAHR)
por: Pastor, Steven, et al.
Publicado: (2020)

Improved Outcomes in Patients with 22q11.2 Deletion Syndrome and Diagnosis of Interrupted Aortic Arch Prior to Birth Hospital Discharge, a Retrospective Study
por: Ron, Hayley A., et al.
Publicado: (2022)

Emergent, remitted and persistent psychosis-spectrum symptoms in 22q11.2 deletion syndrome
por: Tang, S X, et al.
Publicado: (2017)

Altered functional brain dynamics in chromosome 22q11.2 deletion syndrome during facial affect processing
por: Cornblath, Eli J., et al.
Publicado: (2021)

Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DS
por: McDonald-McGinn, Donna M, et al.
Publicado: (2013)

Club foot in association with the 22q11.2 deletion syndrome: An observational study
por: Homans, Jelle F., et al.
Publicado: (2018)

Attention deficit hyperactivity disorder symptoms as antecedents of later psychotic outcomes in 22q11.2 deletion syndrome
por: Niarchou, Maria, et al.
Publicado: (2019)

Speech-Language Disorders in 22q11.2 Deletion Syndrome: Best Practices for Diagnosis and Management
por: Solot, Cynthia B., et al.
Publicado: (2019)

Language Profiles of School-Aged Children with 22q11.2 Copy Number Variants
por: Verbesselt, Jente, et al.
Publicado: (2023)

Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions
por: Blagowidow, Natalie, et al.
Publicado: (2023)

22q11.2 Deletion Syndrome as a Human Model for Idiopathic Scoliosis
por: de Reuver, Steven, et al.
Publicado: (2021)

A catalog of hemizygous variation in 127 22q11 deletion patients
por: Hestand, Matthew S, et al.
Publicado: (2016)

Typical 22q11.2 deletion syndrome appears to confer a reduced risk of schwannoma
por: Evans, D. Gareth, et al.
Publicado: (2021)

Inter-rater reliability of subthreshold psychotic symptoms in individuals with 22q11.2 deletion syndrome
por: Moore, Tyler M., et al.
Publicado: (2021)

Evidence that duplications of 22q11.2 protect against schizophrenia
por: Rees, E, et al.
Publicado: (2014)

Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS
por: Zhao, Yingjie, et al.
Publicado: (2023)

Atypical autism in a boy with double duplication of 22q11.2: implications of increasing dosage
por: Dale, Breanne, et al.
Publicado: (2017)

Clinical experience with single‐nucleotide polymorphism‐based non‐invasive prenatal screening for 22q11.2 deletion syndrome
por: Gross, S. J., et al.
Publicado: (2016)

Characterization of the past and current duplication activities in the human 22q11.2 region
por: Guo, Xingyi, et al.
Publicado: (2011)

Analysis of meiotic recombination in 22q11.2, a region that frequently undergoes deletions and duplications
por: Torres-Juan, Laura, et al.
Publicado: (2007)

Failure to detect the 22q11.2 duplication syndrome rearrangement among patients with schizophrenia
por: Brunet, Anna, et al.
Publicado: (2008)

Opposing white matter microstructure abnormalities in 22q11.2 deletion and duplication carriers
por: Seitz-Holland, Johanna, et al.
Publicado: (2021)

Chromosome 22q11.2 Duplication Syndrome and Diagnostic Overshadowing: A Case Report
por: Singh, Ashok, et al.
Publicado: (2023)

Atypical nested 22q11.2 duplications between LCR22B and LCR22D are associated with neurodevelopmental phenotypes including autism spectrum disorder with incomplete penetrance
por: Woodward, Karen J., et al.
Publicado: (2019)

Deletions and duplications of the 22q11.2 region in spermatozoa from DiGeorge/velocardiofacial fathers
por: Vergés, Laia, et al.
Publicado: (2014)

Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion
por: Cleynen, Isabelle, et al.
Publicado: (2020)

Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3
por: Guo, Tingwei, et al.
Publicado: (2017)

Episodic Behavioural Regression in an 8-Year-Old Female: Sequelae of 22q11.2 Duplication Syndrome
por: Bahji, A., et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_b8ukrrd6kk2ihaquejsvui0vel