(Q42036986)

English

Age estimates of two common mutations causing factor XI deficiency: recent genetic drift is not necessary for elevated disease incidence among Ashkenazi Jews

scientific article published on April 1999

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Europe PubMed Central

PMC publication ID

15 October 2017

Age estimates of two common mutations causing factor XI deficiency: recent genetic drift is not necessary for elevated disease incidence among Ashkenazi Jews (English)

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

1 reference

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Seligsohn U

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

2

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Reich DE

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

author name string

Goldstein DB

1

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

Bradman N

3

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

Usher S

4

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

Peretz H

6

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Europe PubMed Central

PMC publication ID

15 October 2017

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publication date

1 April 1999

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

American Journal of Human Genetics

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Europe PubMed Central

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15 October 2017

64

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Europe PubMed Central

PMC publication ID

15 October 2017

4

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

1071-1075

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

Origins of Old Testament priests

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377831

5 June 2018

Dating the origin of the CCR5-Delta32 AIDS-resistance allele by the coalescence of haplotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377831

5 June 2018

Launching microsatellites: a review of mutation processes and methods of phylogenetic interference

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377831

5 June 2018

The two common mutations causing factor XI deficiency in Jews stem from distinct founders: one of ancient Middle Eastern origin and another of more recent European origin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377831

5 June 2018

Estimating the age of alleles by use of intraallelic variability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377831

5 June 2018

Mutation of human short tandem repeats

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377831

5 June 2018

Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377831

5 June 2018

Failure to detect variant (CRM+) plasma thromboplastin antecedent (factor XI) molecules in hereditary plasma thromboplastin antecedent deficiency: a study of 125 patients of several ethnic backgrounds

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377831

5 June 2018

High gene frequency of factor XI (PTA) deficiency in Ashkenazi Jews

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377831

5 June 2018

One of the two common mutations causing factor XI deficiency in Ashkenazi Jews (type II) is also prevalent in Iraqi Jews, who represent the ancient gene pool of Jews.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377831

17 August 2018

Identifiers

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Europe PubMed Central

PMC publication ID

15 October 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

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