(Q42038259)

15 October 2017

Linkage disequilibrium between the FES, D15S127, and BLM loci in Ashkenazi Jews with Bloom syndrome (English)

1 reference

15 October 2017

1 reference

linkage disequilibrium

1 reference

N A Ellis

1

1 reference

15 October 2017

A M Roe

2

1 reference

15 October 2017

J Kozloski

3

1 reference

15 October 2017

M Proytcheva

4

1 reference

15 October 2017

C Falk

5

1 reference

15 October 2017

J German

6

1 reference

15 October 2017

language of work or name

English

0 references

publication date

1 September 1994

1 reference

American Journal of Human Genetics

15 October 2017

1 reference

15 October 2017

55

1 reference

15 October 2017

3

1 reference

15 October 2017

453-460

1 reference

Systems of Mating. II. the Effects of Inbreeding on the Genetic Composition of a Population

15 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918408

Mapping, cloning and genetic characterization of the region containing the Wilson disease gene.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918408

Refining the position of Wilson disease by linkage disequilibrium with polymorphic microsatellites

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918408

Haplotype studies in Wilson disease

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918408

Bloom syndrome: a mendelian prototype of somatic mutational disease.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918408

Localization of the EPM1 gene for progressive myoclonus epilepsy on chromosome 21: linkage disequilibrium allows high resolution mapping

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918408

Familial Mediterranean fever (FMF) in Moroccan Jews: demonstration of a founder effect by extended haplotype analysis

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918408

Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosis.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918408

Bloom syndrome: an analysis of consanguineous families assigns the locus mutated to chromosome band 15q26.1

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918408

Bloom syndrome: a single complementation group defines patients of diverse ethnic origin.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918408

Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918408

Bloom's syndrome. XII. Report from the Registry for 1987.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918408

Identification of the cystic fibrosis gene: genetic analysis

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918408

Tetranucleotide repeat polymorphism at the human c-fes/fps proto-oncogene (FES)

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918408

Complex patterns of linkage disequilibrium in the Huntington disease region

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918408

A positive selection vector for cloning high molecular weight DNA by the bacteriophage P1 system: improved cloning efficacy

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918408

Elevated sister chromatid exchange phenotype of Bloom syndrome cells is complemented by human chromosome 15

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918408

Strong allelic association between the torsion dystonia gene (DYT1) andloci on chromosome 9q34 in Ashkenazi Jews

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918408

Friedreich ataxia in Louisiana Acadians: demonstration of a founder effect by analysis of microsatellite-generated extended haplotypes

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918408

Bloom's syndrome. VI. The disorder in Israel and an estimation of the gene frequency in the Ashkenazim

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918408

Normalisation of sister chromatid exchange frequencies in Bloom's syndrome by euploid cell hybridisation

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918408

Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918408

Localization of the cellular oncogenes ABL, SIS, and FES on human germ-line chromosomes

27 July 2018

1 reference

12 December 2020

Confirmation of 15q26.1 as the site of the FES protooncogene by fluorescence in situ hybridization

1 reference

12 December 2020

A linkage map of human chromosome 15 with an average resolution of 2 cM and containing 55 polymorphic microsatellites

1 reference

12 December 2020

8 The population genetics of the haemoglobinopathies

1 reference

12 December 2020

Identifiers

1 reference

15 October 2017

PubMed publication ID

8079989

1 reference