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99 Artículos relativos a Efecto Fundador-
- High incidence of central nervous system malformations associated with marked parental consanguinity in an Israeli Arab community.
Publicado en Biomed Pharmacother - The high frequency of the Hb B2 variant in the Herero population: a founder effect?.
Publicado en Hemoglobin - Comparative study of Fanconi anemia in children of different ethnic origin in South Africa.
Publicado en Am J Med Genet - Assignment of a gene for autosomal recessive retinitis pigmentosa (RP12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease population.
Publicado en Genomics - The fragile X syndrome in Finland: demonstration of a founder effect by analysis of microsatellite haplotypes.
Publicado en Hum Genet - Molecular biogeography of clonal lineages in a high-arctic apomictic Daphnia complex.
Publicado en Mol Ecol - Distribution of FMR-1 and associated microsatellite alleles in a normal Chinese population.
Publicado en Am J Med Genet - Haplotype analysis at the FRAXA locus in the Japanese population.
Publicado en Am J Med Genet - Fragile X founder chromosome effects: linkage disequilibrium or microsatellite heterogeneity?.
Publicado en Am J Med Genet - Population genetics of phenylketonuria.
Publicado en Acta Paediatr Suppl - Familial hyperinsulinism maps to chromosome 11p14-15.1, 30 cM centromeric to the insulin gene.
Publicado en Nat Genet - Proenkephalin transgenic mice: a short promoter confers high testis expression and reduced fertility.
Publicado en Mol Reprod Dev - Molecular evolution and population genetics of Greater Caribbean green turtles (Chelonia mydas) as inferred from mitochondrial DNA control region sequences.
Publicado en Genetica - Linkage analysis in two schizophrenic families originating from a restricted subpopulation of Finland.
Publicado en Psychiatr Genet - Rett syndrome: potential gene sources--phenotypical variability.
Publicado en Clin Genet - Mitochondrial DNA variation and population genetic structure of the northern redbelly dace (Phoxinus eos).
Publicado en Mol Ecol - Genetic consequences of differential demographic behaviour in the Saguenay region, Québec.
Publicado en Am J Phys Anthropol - Mutation of the glucagon receptor gene and diabetes mellitus in the UK: association or founder effect?.
Publicado en Hum Mol Genet - Molecular analysis in factor XIIIA deficiency.
Publicado en Thromb Haemost - Founding mutations and Alu-mediated recombination in hereditary colon cancer.
Publicado en Nat Med - Molecular epidemiology of factor IX germline mutations in Mexican Hispanics: pattern of mutation and potential founder effects.
Publicado en Thromb Haemost - Geographic and ethnic distributions of the more frequent cystic fibrosis mutations in Europe show that a founder effect is apparent for several mutant alleles.
Publicado en Hum Biol - CDKN2 explains part of the clinical phenotype in Dutch familial atypical multiple-mole melanoma (FAMMM) syndrome families.
Publicado en Melanoma Res - Recurrent LDL-receptor mutation causes familial hypercholesterolaemia in South African coloureds and Afrikaners.
Publicado en S Afr Med J - Familial defective apolipoprotein-B is rare in hypercholesterolaemic South African Afrikaners, coloureds and Indians.
Publicado en S Afr Med J - Mhc-DRB genes and the origin of New World monkeys.
Publicado en Mol Phylogenet Evol - Recombinant mapping of the familial hyperinsulinism gene to an 0.8 cM region on chromosome 11p15.1 and demonstration of a founder effect in Ashkenazi Jews.
Publicado en Hum Mol Genet - Enzyme polymorphism among Triatoma infestans (Hemiptera: Reduviidae) colonies.
Publicado en J Med Entomol - Familial amyloid polyneuropathy (TTR ala 60) in north west Ireland: a clinical, genetic, and epidemiological study.
Publicado en J Neurol Neurosurg Psychiatry - Genetic mapping of the spinocerebellar ataxia 2 (SCA2) locus on chromosome 12q23-q24.1.
Publicado en Genomics - High incidence of cystic fibrosis on the Faroe Islands: a molecular and genealogical study.
Publicado en Hum Genet - Mitochondrial and nuclear genetic contribution of female founders to a contemporary population in northeast Quebec.
Publicado en Am J Hum Genet - A common gene for juvenile and adult-onset primary open-angle glaucomas confined on chromosome 1q.
Publicado en Am J Hum Genet - New founder haplotypes at the myotonic dystrophy locus in southern Africa.
Publicado en Am J Hum Genet - Ethnic distribution of the fragile X syndrome in Israel: evidence of founder chromosomes(?).
Publicado en Isr J Med Sci - Von Hippel-Lindau (VHL) disease with pheochromocytoma in the Black Forest region of Germany: evidence for a founder effect.
Publicado en Hum Genet - Prevalence and founder effect of Huntington's disease in the San-in area of Japan.
Publicado en Rinsho Shinkeigaku - Mitochondrial DNA of the Mauritian macaques (Macaca fascicularis): an example of the founder effect.
Publicado en Am J Phys Anthropol - Indo-European origins: a computer-simulation test of five hypotheses.
Publicado en Am J Phys Anthropol - Activation of expression of multiple subfamilies of human Alu elements by adenovirus type 5 and herpes simplex virus type 1.
Publicado en J Mol Biol - Molecular basis of late infantile metachromatic leukodystrophy in the Habbanite Jews.
Publicado en Hum Mutat - Preliminary investigation of mutations in 21-hydroxylase gene in patients with congenital adrenal hyperplasia in Russia.
Publicado en Hum Mutat - The high frequency of the -6G-->A factor IX promoter mutation is the result both of a founder effect and recurrent mutation at a CpG dinucleotide.
Publicado en Br J Haematol - Arthrogryposis multiplex congenita in an Arab kindred: update.
Publicado en Am J Med Genet - MtDNA haplogroups in Native Americans.
Publicado en Am J Hum Genet - Wilson disease in Iceland: a clinical and genetic study.
Publicado en Am J Hum Genet - Size of genetic bottlenecks leading to virus fitness loss is determined by mean initial population fitness.
Publicado en J Virol - A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17.
Publicado en Nat Genet - Transthyretin Ser 6 gene frequency in individuals without amyloidosis.
Publicado en Hum Genet - Haplotype analysis in Australian hemochromatosis patients: evidence for a predominant ancestral haplotype exclusively associated with hemochromatosis.
Publicado en Am J Hum Genet - Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families.
Publicado en Am J Hum Genet - PCR amplification of intergenic spacers in the ribosomal DNA of Drosophila melanogaster reveals high levels of turnover in length and copy-number of spacers in geographically separated populations.
Publicado en Mol Ecol - Refined mapping of the Usher syndrome type III locus on chromosome 3, exclusion of candidate genes, and identification of the putative mouse homologous region.
Publicado en Genomics - The Réunion paradox and the digenic model.
Publicado en Am J Hum Genet - High mitochondrial sequence diversity in linguistic isolates of the Alps.
Publicado en Am J Hum Genet - Linkage-disequilibrium mapping narrows the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region to <100 kb.
Publicado en Am J Hum Genet - Mutations in the sulonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews.
Publicado en Hum Mol Genet - Microsatellite differentiation between Phillip Island and mainland Australian populations of the red fox Vulpes vulpes.
Publicado en Mol Ecol - Origin and migration of an Afrikaner founder mutation FHAfrikaner-2 (V408M) causing familial hypercholesterolemia.
Publicado en Gene Geogr - Protein trafficking violations.
Publicado en Nat Genet - DNA fingerprinting of captive breeding pairs of lesser white-fronted geese (Anser erythropus) with unknown pedigrees.
Publicado en Biochem Genet - The mutations and VNTRs in the phenylalanine hydroxylase gene of phenylketonuria in St Petersburg.
Publicado en J Inherit Metab Dis - Genetic screening in hereditary multiple endocrine neoplasia type 1: absence of a founder effect among Japanese families.
Publicado en Jpn J Cancer Res - The factor IX gene as a model for analysis of human germline mutations: an update.
Publicado en Hum Mol Genet - No founder effect in three novel Alzheimer's disease families with APP 717 Val-->Ile mutation. Clerget-darpoux. French Alzheimer's Disease Study Group.
Publicado en J Med Genet - The peopling of the Americas.
Publicado en Science - Gene mapping in Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24.
Publicado en Nat Genet - Random genetic drift in the female germline explains the rapid segregation of mammalian mitochondrial DNA.
Publicado en Nat Genet - Expression of the murine wild-type tyrosinase gene in transgenic rabbits.
Publicado en Transgenic Res - Fragile X founder effects and new mutations in Finland.
Publicado en Am J Med Genet - Fragile X founder chromosomes in Italy: a few initial events and possible explanation for their heterogeneity.
Publicado en Am J Med Genet - Seventh International Workshop on the Fragile X and X-linked Mental Retardation.
Publicado en Am J Med Genet - Identification of three mutations and associated haplotypes in the protoporphyrinogen oxidase gene in South African families with variegate porphyria.
Publicado en Hum Mol Genet - Origin and evolution of Native American mtDNA variation: a reappraisal.
Publicado en Am J Hum Genet - Hypokalemic periodic paralysis mutations: confirmation of mutation and analysis of founder effect.
Publicado en Neuromuscul Disord - Recurrence of the PROC gene mutation R178Q: independent origins in Spanish protein C deficiency patients.
Publicado en Hum Mutat - Population stratifications can cause false positive linkage results if founders are untyped.
Publicado en Ann Hum Genet - Identity-by-descent mapping of recessive traits in livestock: application to map the bovine syndactyly locus to chromosome 15.
Publicado en Genome Res - Linkage disequilibrium analysis in young populations: pseudo-vitamin D-deficiency rickets and the founder effect in French Canadians.
Publicado en Am J Hum Genet - Localization of the familial Mediterranean fever gene (FMF) to a 250-kb interval in non-Ashkenazi Jewish founder haplotypes. The French FMF Consortium.
Publicado en Am J Hum Genet - A common BRCA1 mutation in Norwegian breast and ovarian cancer families?.
Publicado en Am J Hum Genet - Founder effect and prevalence of myotonic dystrophy in South Africans: molecular studies.
Publicado en Am J Hum Genet - Natural selection and random genetic drift as causes of evolution on islands.
Publicado en Philos Trans R Soc Lond B Biol Sci - Small mammal differentiation on islands.
Publicado en Philos Trans R Soc Lond B Biol Sci - APC intragenic haplotypes in familial adenomatous polyposis.
Publicado en Clin Genet - Asthma on Tristan da Cunha: looking for the genetic link. The University of Toronto Genetics of Asthma Research Group.
Publicado en Am J Respir Crit Care Med - Mitochondrial DNA analysis of Mongolian populations and implications for the origin of New World founders.
Publicado en Genetics - The four founding lineage hypothesis for the New World: a critical reevaluation.
Publicado en Mol Phylogenet Evol - Private polymorphisms: how many? How old? How useful for genetic taxonomies?.
Publicado en Mol Phylogenet Evol - mtDNA variation in the Yanomami: evidence for additional New World founding lineages.
Publicado en Am J Hum Genet - mtDNA variation indicates Mongolia may have been the source for the founding population for the New World.
Publicado en Am J Hum Genet - Ataxia-telangiectasia: mutations in ATM cDNA detected by protein-truncation screening.
Publicado en Am J Hum Genet - A hierarchical analysis of population genetic structure in Rhizobium leguminosarum bv. trifolii.
Publicado en Mol Ecol - High-level expression of recombinant human fibrinogen in the milk of transgenic mice.
Publicado en Nat Biotechnol - The age of human mutation: genealogical and linkage disequilibrium analysis of the CLN5 mutation in the Finnish population.
Publicado en Am J Hum Genet - Founding BRCA1 mutations in hereditary breast and ovarian cancer in southern Sweden.
Publicado en Am J Hum Genet - Contrasting in vivo effects of murine and human apolipoprotein A-II. Role of monomer versus dimer.
Publicado en J Biol Chem - The effects of social structure, geographical structure, and population size on the evolution of mitochondrial DNA: I. A simulation model.
Publicado en Comput Appl Biosci - Mutations in the founder of the MIP gene family underlie cataract development in the mouse.
Publicado en Nat Genet
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