(Q24670504)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8102508%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

title

Genetic heterogeneity in benign familial neonatal convulsions: identification of a new locus on chromosome 8q (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8102508%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

1 reference

1 reference

T B Lewis

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8102508%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

R J Leach

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8102508%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

K Ward

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8102508%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

P O'Connell

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8102508%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

S G Ryan

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8102508%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

language of work or name

English

0 references

publication date

1 September 1993

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8102508%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

25 October 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8102508%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

volume

53

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8102508%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

page(s)

670-675

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8102508%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8102508%20AND%20SRC:MED&resulttype=core&format=json

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

25 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682419

Detection of specific sequences among DNA fragments separated by gel electrophoresis

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682419

Benign familial neonatal convulsions: Evidence for clinical and genetic heterogeneity

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682419

Polymorphic DNA region adjacent to the 5' end of the human insulin gene

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682419

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682419

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682419

28 September 2017

Benign neonatal seizures

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682419

A second-generation linkage map of the human genome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682419

Benign familial neonatal convulsions linked to genetic markers on chromosome 20.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682419

Dinucleotide repeat polymorphism at the human c-myc oncogene locus (MYC)

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682419

Benign familial convulsions in the neonatal period and early infancy

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682419

Confirmation of linkage of benign familial neonatal convulsions to D20S19 and D20S20.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682419

Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines

19 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682419

Benign familial neonatal seizures: clinical and electroencephalographic characteristics

28 November 2018

1 reference

12 December 2020

A simple scheme for the analysis of HLA linkages in pedigrees

1 reference

12 December 2020

Dominant benign neonatal seizures

1 reference

12 December 2020

The risks of seizure disorders among relatives of patients with childhood onset epilepsy

1 reference

12 December 2020

Benign familial neonatal convulsions

1 reference

12 December 2020

Benign familial neonatal-infantile seizures

1 reference

12 December 2020

Familial neonatal and infantile seizures: an autosomal-dominant disorder

1 reference

12 December 2020

Mapping of human chromosome 5 microsatellite DNA polymorphisms

1 reference

12 December 2020

A comprehensive genetic linkage map of the human genome. NIH/CEPH Collaborative Mapping Group

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8102508%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

1 reference