(Q35726686)

9 August 2017

title

Absence seizures with intellectual disability as a phenotype of the 15q13.3 microdeletion syndrome (English)

1 reference

disability affecting intellectual abilities

9 August 2017

0 references

intellectual disability

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based on heuristic

inferred from title

1 reference

1 reference

2

Heather C Mefford

1 reference

9 August 2017

5

Evan E Eichler

1 reference

9 August 2017

3

Tanja Obermeier

1 reference

9 August 2017

1

Hiltrud Muhle

1 reference

9 August 2017

Sarah von Spiczak

4

1 reference

9 August 2017

Ulrich Stephani

series ordinal

6

1 reference

9 August 2017

Thomas Sander

series ordinal

7

1 reference

9 August 2017

Ingo Helbig

series ordinal

8

1 reference

9 August 2017

publication date

2 November 2011

1 reference

9 August 2017

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9 August 2017

volume

52

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9 August 2017

issue

12

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9 August 2017

page(s)

e194-8

1 reference

Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies

9 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270691

Finding the missing heritability of complex diseases

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270691

Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270691

Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270691

15q13.3 microdeletions increase risk of idiopathic generalized epilepsy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270691

Large recurrent microdeletions associated with schizophrenia

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270691

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270691

Familial occurrence of early-onset childhood absence epilepsy.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270691

A proposed diagnostic scheme for people with epileptic seizures and with epilepsy: report of the ILAE Task Force on Classification and Terminology

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270691

Childhood absence epilepsy with clinically apparent genetic and acquired burdens: a diagnostic consideration

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270691

10.1111/J.1528-1167.2011.03301.X

25 September 2018

Identifiers

DOI

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9 August 2017

1 reference

9 August 2017

1 reference