Pages that link to "Q42036986"

The following pages link to Age estimates of two common mutations causing factor XI deficiency: recent genetic drift is not necessary for elevated disease incidence among Ashkenazi Jews (Q42036986):

Displaying 32 items.

• Geographic distribution of disease mutations in the Ashkenazi Jewish population supports genetic drift over selection (Q24532103) (← links)
• A population-genetic test of founder effects and implications for Ashkenazi Jewish diseases (Q24534086) (← links)
• Y chromosomes traveling south: the cohen modal haplotype and the origins of the Lemba--the "Black Jews of Southern Africa" (Q24539055) (← links)
• Gaucher disease: the origins of the Ashkenazi Jewish N370S and 84GG acid beta-glucosidase mutations (Q24540255) (← links)
• Genetic evidence for different male and female roles during cultural transitions in the British Isles (Q24607088) (← links)
• Contrasting patterns of Y chromosome variation in Ashkenazi Jewish and host non-Jewish European populations (Q28240347) (← links)
• Microsatellite variation and evolution of human lactase persistence (Q28253975) (← links)
• 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 (Q28363162) (← links)
• Age estimate of the N370S mutation causing Gaucher disease in Ashkenazi Jews and European populations: A reappraisal of haplotype data (Q30586774) (← links)
• Detecting population growth, selection and inherited fertility from haplotypic data in humans (Q30885928) (← links)
• Tracing the origin of the most common thiopurine methyltransferase (TPMT) variants: preliminary data from the patterns of haplotypic association with two CA repeats. (Q30940248) (← links)
• Combined use of biallelic and microsatellite Y-chromosome polymorphisms to infer affinities among African populations (Q33870486) (← links)
• Genetic anthropology of the colorectal cancer-susceptibility allele APC I1307K: evidence of genetic drift within the Ashkenazim (Q33905286) (← links)
• MtDNA evidence for a genetic bottleneck in the early history of the Ashkenazi Jewish population (Q34289752) (← links)
• Origin and spread of the 1278insTATC mutation causing Tay-Sachs disease in Ashkenazi Jews: genetic drift as a robust and parsimonious hypothesis (Q34290326) (← links)
• A 122.5-kilobase deletion of the P gene underlies the high prevalence of oculocutaneous albinism type 2 in the Navajo population (Q34354851) (← links)
• Impact of BRCA mutations on female fertility and offspring sex ratio (Q34994757) (← links)
• LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago. (Q35070498) (← links)
• 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 A (Q35549086) (← links)
• A Bayesian method for jointly estimating allele age and selection intensity (Q37090546) (← links)
• Coagulation disorders and inhibitors of coagulation in children from Mansoura, Egypt (Q38855974) (← links)
• Identification and population history of CYP4V2 mutations in patients with Bietti crystalline corneoretinal dystrophy (Q40397099) (← links)
• A novel RLBP1 gene geographical area-related mutation present in a young patient with retinitis punctata albescens (Q41211593) (← links)
• Type I mutation in the F11 gene is a third ancestral mutation which causes factor XI deficiency in Ashkenazi Jews (Q43498244) (← links)
• NOD2/CARD15 genotype and phenotype differences between Ashkenazi and Sephardic Jews with Crohn's disease (Q47387930) (← links)
• High-throughput analysis of informative CYP2D6 compound haplotypes (Q47405014) (← links)
• A genetic profile of contemporary Jewish populations (Q47596505) (← links)
• A common ancestral mutation (C128X) occurring in 11 non-Jewish families from the UK with factor XI deficiency (Q47613885) (← links)
• Age and origin of the FCMD 3'-untranslated-region retrotransposal insertion mutation causing Fukuyama-type congenital muscular dystrophy in the Japanese population (Q47644883) (← links)
• Microsatellite variation and evolution of the human Duffy blood group polymorphism (Q48281952) (← links)
• Factor XI deficiency (Q56335014) (← links)
• Population Genetics of the Ashkenazim (Q56536343) (← links)