(Q34387487)

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Childhood absence epilepsy with tonic-clonic seizures and electroencephalogram 3-4-Hz spike and multispike-slow wave complexes: linkage to chromosome 8q24.

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Europe PubMed Central

PubMed publication ID

1 August 2017

Childhood absence epilepsy with tonic-clonic seizures and electroencephalogram 3-4-Hz spike and multispike-slow wave complexes: linkage to chromosome 8q24. (English)

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Europe PubMed Central

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1 August 2017

childhood absence epilepsy

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based on heuristic

inferred from title

12

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L J Treiman

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1 August 2017

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G C Fong

1

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1 August 2017

P U Shah

2

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1 August 2017

M N Gee

3

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Europe PubMed Central

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1 August 2017

J M Serratosa

4

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Europe PubMed Central

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1 August 2017

I P Castroviejo

5

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Europe PubMed Central

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1 August 2017

S Khan

6

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1 August 2017

S H Ravat

7

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Europe PubMed Central

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1 August 2017

J Mani

8

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1 August 2017

Y Huang

9

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1 August 2017

H Z Zhao

10

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1 August 2017

M T Medina

11

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1 August 2017

G Pineda

13

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1 August 2017

A V Delgado-Escueta

14

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1 August 2017

language of work or name

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publication date

1 October 1998

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1 August 2017

American Journal of Human Genetics

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1 August 2017

63

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1 August 2017

4

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Europe PubMed Central

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1 August 2017

1117-1129

1 reference

Europe PubMed Central

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1 August 2017

Sequential tests for the detection of linkage

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377498

6 July 2018

Clinical and genetic analysis of a large pedigree with juvenile myoclonic epilepsy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377498

6 July 2018

Localization of a gene for a glutamate binding subunit of a NMDA receptor (GRINA) to 8q24.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377498

6 July 2018

A comprehensive genetic map of the human genome based on 5,264 microsatellites

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377498

6 July 2018

Linkage analysis of idiopathic generalized epilepsy (IGE) and marker loci on chromosome 6p in families of patients with juvenile myoclonic epilepsy: no evidence for an epilepsy locus in the HLA region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377498

6 July 2018

Juvenile myoclonic epilepsy locus in chromosome 6p21.2-p11: linkage to convulsions and electroencephalography trait

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377498

6 July 2018

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377498

6 July 2018

A YAC contig map of the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377498

6 July 2018

Epileptic seizures caused by inactivation of a novel gene, jerky, related to centromere binding protein-B in transgenic mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377498

6 July 2018

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377498

6 July 2018

The affected-pedigree-member method of linkage analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377498

6 July 2018

Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377498

6 July 2018

A note on multiple testing procedures in linkage analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377498

6 July 2018

Localization of idiopathic generalized epilepsy on chromosome 6p in families of juvenile myoclonic epilepsy patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377498

6 July 2018

Nomenclature for mammalian potassium channel genes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377498

27 October 2018

Mapping of genes predisposing to idiopathic generalized epilepsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/9758624

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics of convulsive disorders. II. Genetic and electroencephalographic studies in centrencephalic epilepsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/9758624

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epidemiology of different types of epilepsy in school age children of Modena, Italy

1 reference

https://pubmed.ncbi.nlm.nih.gov/9758624

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

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