(Q35195036)

English

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

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scholarly article

1 reference

Europe PubMed Central

7 August 2017

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 (English)

1 reference

Europe PubMed Central

7 August 2017

myoclonic epilepsy

1 reference

based on heuristic

inferred from title

juvenile myoclonic epilepsy

1 reference

based on heuristic

inferred from title

author name string

W P Whitehouse

1

1 reference

Europe PubMed Central

7 August 2017

M Rees

2

1 reference

Europe PubMed Central

7 August 2017

D Curtis

3

1 reference

Europe PubMed Central

7 August 2017

A Sundqvist

4

1 reference

Europe PubMed Central

7 August 2017

K Parker

5

1 reference

Europe PubMed Central

7 August 2017

E Chung

6

1 reference

Europe PubMed Central

7 August 2017

D Baralle

7

1 reference

Europe PubMed Central

7 August 2017

R M Gardiner

8

1 reference

Europe PubMed Central

7 August 2017

language of work or name

0 references

publication date

1 September 1993

1 reference

Europe PubMed Central

7 August 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

7 August 2017

53

1 reference

Europe PubMed Central

7 August 2017

652-662

1 reference

Europe PubMed Central

7 August 2017

3

1 reference

Europe PubMed Central

7 August 2017

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682418

28 July 2018

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682418

28 July 2018

Construction of a map of the short arm of human chromosome 6

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682418

28 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=1682418

28 July 2018

Extensive DNA polymorphism at the factor XIIIa (F13A) locus and linkage to HLA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682418

28 July 2018

Dinucleotide repeat polymorphism at the D6S89 locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682418

28 July 2018

Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682418

28 July 2018

Assessing the effect of multiple linkage tests in complex diseases.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682418

28 July 2018

Measuring the inflation of the lod score due to its maximization over model parameter values in human linkage analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682418

28 July 2018

Genetic linkage and complex diseases, with special reference to psychiatric disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682418

28 July 2018

Gene mapping in the idiopathic generalized epilepsies: juvenile myoclonic epilepsy, childhood absence epilepsy, epilepsy with grand mal seizures, and early childhood myoclonic epilepsy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682418

28 July 2018

Dinucleotide repeat polymorphism at the D6S109 locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682418

28 July 2018

Dinucleotide repeat polymorphism at the D6S105 locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682418

28 July 2018

HLA class II genes: typing by DNA analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682418

28 July 2018

Polymorphism of the human complement component C4.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682418

28 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=1682418

28 July 2018

Linkage mapping and fluorescence in situ hybridization of TCTE1 on human chromosome 6p: analysis of dinucleotide polymorphisms on native gels.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682418

28 July 2018

Confirmation of linkage between juvenile myoclonic epilepsy locus and the HLA region of chromosome 6.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682418

28 July 2018

A procedure for combining two-point lod scores into a summary multipoint map.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682418

27 September 2018

Man bites dog? The validity of maximizing lod scores to determine mode of inheritance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682418

27 September 2018

Cutting a Gordian knot in the linkage analysis of complex human traits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682418

27 September 2018

Juvenile myoclonic epilepsy (JME) may be linked to the BF and HLA loci on human chromosome 6

1 reference

https://pubmed.ncbi.nlm.nih.gov/8352275

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Juvenile myoclonic epilepsy: an autosomal recessive disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8352275

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inferring mode of inheritance by comparison of lod scores

1 reference

https://pubmed.ncbi.nlm.nih.gov/8352275

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On the genetics of the primary generalized epilepsy with sporadic myoclonias of impulsive petit mal type. A clinical and electroencephalographic study of 399 probands

1 reference

https://pubmed.ncbi.nlm.nih.gov/8352275

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

7 August 2017

1 reference

Europe PubMed Central

7 August 2017

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