Childhood-Onset Schizophrenia: A Systematic Overview of Its Genetic Heterogeneity From Classical Studies to the Genomic Era (Q92539390)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31921276 AND SRC:MED&resulttype=core&format=json

30 April 2020

review article

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title

Childhood-Onset Schizophrenia: A Systematic Overview of Its Genetic Heterogeneity From Classical Studies to the Genomic Era (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31921276 AND SRC:MED&resulttype=core&format=json

30 April 2020

1 reference

1

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30 April 2020

Barbara Bardoni

7

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30 April 2020

author name string

Malgorzata Marta Drozd

2

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30 April 2020

Susanne Thümmler

3

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30 April 2020

Emmanuelle Dor

4

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30 April 2020

Maria Capovilla

5

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30 April 2020

Florence Askenazy

6

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30 April 2020

publication date

18 December 2019

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30 April 2020

published in

Frontiers in Genetics

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30 April 2020

volume

10

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30 April 2020

page(s)

1137

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Creative Commons Attribution 4.0 International

30 April 2020

copyright license

start time

18 December 2019

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April 2022 Public Data File from Crossref

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11 February 2021

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11 February 2021

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11 February 2021

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11 February 2021

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11 February 2021

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Childhood-onset schizophrenia/autistic disorder and t(1;7) reciprocal translocation: identification of a BAC contig spanning the translocation breakpoint at 7q21.

11 February 2021

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Childhood-onset schizophrenia: rare but worth studying

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Clinical and neurobiological correlates of cytogenetic abnormalities in childhood-onset schizophrenia

11 February 2021

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Autosomal dominant cerebellar ataxia type III: linkage in a large British family to a 7.6-cM region on chromosome 15q14-21.3.

11 February 2021

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Large CAG/CTG repeats are associated with childhood-onset schizophrenia

11 February 2021

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Brief Report: Association of Sex Chromosome Anomalies With Childhood-Onset Psychotic Disorders

11 February 2021

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Chromosome 22q11.2 interstitial deletions among childhood-onset schizophrenics and "multidimensionally impaired".

11 February 2021

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A homozygous mutation in the integrin alpha6 gene in junctional epidermolysis bullosa with pyloric atresia

11 February 2021

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Absence of integrin alpha 6 leads to epidermolysis bullosa and neonatal death in mice

11 February 2021

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Brief report: translocation involving chromosomes 1 and 7 in a boy with childhood-onset schizophrenia

11 February 2021

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Autistic children who become schizophrenic

11 February 2021

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A North Dakota prevalence study of schizophrenia presenting in childhood

11 February 2021

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Localization of a human Na ,K -ATPase alpha subunit gene to chromosome 19q12----q13.2 and linkage to the myotonic dystrophy locus

11 February 2021

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Molecular cloning of the human alpha 6 integrin subunit. Alternative splicing of alpha 6 mRNA and chromosomal localization of the alpha 6 and beta 4 genes

11 February 2021

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6930680

11 February 2021

Identifiers

DOI

10.3389/FGENE.2019.01137

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31921276 AND SRC:MED&resulttype=core&format=json

30 April 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31921276 AND SRC:MED&resulttype=core&format=json

30 April 2020

PubMed publication ID

31921276

1 reference