| scholarly article | Q13442814 |
| P50 | author | David Reich | Q5238967 |
| Uri Seligsohn | Q12403602 | ||
| P2093 | author name string | Bradman N | |
| Goldstein DB | |||
| Peretz H | |||
| Usher S | |||
| P2860 | cites work | Dating the origin of the CCR5-Delta32 AIDS-resistance allele by the coalescence of haplotypes | Q24538942 |
| Mutation of human short tandem repeats | Q34357335 | ||
| Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population | Q34722031 | ||
| 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 | Q39192187 | ||
| Launching microsatellites: a review of mutation processes and methods of phylogenetic interference | Q41649401 | ||
| Estimating the age of alleles by use of intraallelic variability | Q43109079 | ||
| 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 | Q44492859 | ||
| 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. | Q44519505 | ||
| Origins of Old Testament priests | Q44583414 | ||
| High gene frequency of factor XI (PTA) deficiency in Ashkenazi Jews | Q44740745 | ||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | genetic drift | Q486420 |
| P304 | page(s) | 1071-1075 | |
| P577 | publication date | 1999-04-01 | |
| P1433 | published in | American Journal of Human Genetics | Q4744249 |
| P1476 | title | Age estimates of two common mutations causing factor XI deficiency: recent genetic drift is not necessary for elevated disease incidence among Ashkenazi Jews | |
| P478 | volume | 64 |
| Q34354851 | A 122.5-kilobase deletion of the P gene underlies the high prevalence of oculocutaneous albinism type 2 in the Navajo population |
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| Q47405014 | High-throughput analysis of informative CYP2D6 compound haplotypes |
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| Q28363162 | Recent origin and spread of a common Lithuanian mutation, G197del LDLR, causing familial hypercholesterolemia: positive selection is not always necessary to account for disease incidence among Ashkenazi Jews |
| Q35549086 | Tay-Sachs disease preconception screening in Australia: self-knowledge of being an Ashkenazi Jew predicts carrier state better than does ancestral origin, although there is an increased risk for c.1421 + 1G > C mutation in individuals with South Afr |
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| Q43498244 | Type I mutation in the F11 gene is a third ancestral mutation which causes factor XI deficiency in Ashkenazi Jews |
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