(Q50312859)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21302354%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

title

Narrowing the critical deletion region for autism spectrum disorders on 16p11.2. (English)

1 reference

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22 January 2020

main subject

autism spectrum disorder

0 references

0 references

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21302354%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

Ilse Noens

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21302354%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

Hilde Peeters

8

1 reference

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22 January 2020

author name string

An Crepel

1

1 reference

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22 January 2020

Wouter De la Marche

3

1 reference

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22 January 2020

Veerle De Wolf

4

1 reference

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22 January 2020

Jean-Pierre Fryns

5

1 reference

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22 January 2020

Koen Devriendt

7

1 reference

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22 January 2020

publication date

11 January 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21302354%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

22 January 2020

published in

1 reference

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22 January 2020

volume

156

1 reference

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22 January 2020

issue

2

1 reference

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22 January 2020

page(s)

243-245

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21302354%20AND%20SRC:MED&resulttype=core&format=json

Gene prioritization through genomic data fusion

22 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31163

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31163

Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31163

Recurrent 16p11.2 microdeletions in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31163

Association and mutation analyses of 16p11.2 autism candidate genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31163

Structural variation of chromosomes in autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31163

Confirmation study of PTEN mutations among individuals with autism or developmental delays/mental retardation and macrocephaly.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31163

Microduplications of 16p11.2 are associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31163

Nuclear localization of PTEN is regulated by Ca(2+) through a tyrosil phosphorylation-independent conformational modification in major vault protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31163

Disturbance of cerebellar synaptic maturation in mutant mice lacking BSRPs, a novel brain-specific receptor-like protein family

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31163

Vault ribonucleoprotein particles: sarcophagi, gondolas, or safety deposit boxes?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31163

Association between microdeletion and microduplication at 16p11.2 and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31163

PTEN associates with the vault particles in HeLa cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31163

21 January 2018

Identifiers

DOI

10.1002/AJMG.B.31163

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21302354%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

1 reference