(Q24642799)

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2220022

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2220022

Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2220022

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2220022

Utilization of lymphoblastoid cell lines as a system for the molecular modeling of autism

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2220022

Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2220022

Ethics. Incidental findings in brain imaging research

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2220022

Genomic and functional profiling of duplicated chromosome 15 cell lines reveal regulatory alterations in UBE3A-associated ubiquitin-proteasome pathway processes

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2220022

Genomic microarray analysis identifies candidate loci in patients with corpus callosum anomalies.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2220022

Microarray based comparative genomic hybridization testing in deletion bearing patients with Angelman syndrome: genotype-phenotype correlations

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2220022

What makes clinical research ethical?

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2220022

The therapeutic misconception: informed consent in psychiatric research

27 September 2017

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2220022

27 September 2017

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181485688

Discovery and disclosure of incidental findings in neuroimaging research

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2220022

Ethical and practical considerations in the management of incidental findings in pediatric MRI studies.

30 May 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181485688

Incidental findings on brain magnetic resonance imaging from 1000 asymptomatic volunteers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181485688

15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181485688

An atypical deletion of the Williams-Beuren syndrome interval implicates genes associated with defective visuospatial processing and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181485688

Pure de-novo 5 Mb duplication at Xp11.22-p11.23 in a male: phenotypic and molecular characterization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181485688

Bioethics: dial 'E' for ethics

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181485688

Array-based comparative genomic hybridization analysis of recurrent chromosome 15q rearrangements

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181485688

Ethical ramifications of genetic analysis using DNA arrays

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2220022

28 November 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/17873651

12 December 2020

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/17873651

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1097/GIM.0B013E3181485688

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/y7rkcmbysbf35l3trvivntufhq

30 July 2022

Dimensions Publication ID

1031501325

0 references

Fatcat ID

release_y7rkcmbysbf35l3trvivntufhq

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/y7rkcmbysbf35l3trvivntufhq

30 July 2022

https://api.fatcat.wiki/v0/release/y7rkcmbysbf35l3trvivntufhq

1 reference

30 July 2022

https://api.fatcat.wiki/v0/release/y7rkcmbysbf35l3trvivntufhq

PubMed publication ID

1 reference

30 July 2022