Low Frequency of the ΔF508 Mutation in Finno-Ugrian and Baltic PopulationsLinkage analysis in the next-generation sequencing eraWhere's the evidence?The API2/MALT1 fusion product may lead to germinal center B cell lymphomas by suppression of apoptosisAssociations between genetic variants in the NOS1AP (CAPON) gene and cardiac repolarization in the old order AmishCoordinated conditional simulation with SLINK and SUP of many markers linked or associated to a trait in large pedigreesAnalysis of 30 genes (355 SNPS) related to energy homeostasis for association with adiposity in European-American and Yup'ik Eskimo populationsPhenome-Wide Association Studies: Embracing Complexity for DiscoveryDrivers of cousin marriage among British PakistanisPhysical and cDNA mapping in the DBH region of human chromosome 9q34Gene mapping in isolated populations: new roles for old friends?A statistically valid alternative to the TDTFLJ14813 missense mutation: a candidate for autosomal dominant thrombocytopenia on human chromosome 10Y-chromosomal diversity suggests that Baltic males share common Finno-Ugric-speaking forefathersHaemochromatosis gene mutations in Finns, Swedes and Swedish SaamisDistribution of rhesus blood group system in the French basques: a reappraisal using the allele-specific primers PCR methodLocal population structure in Arabian Peninsula revealed by Y-STR diversityLinkage relations of the phenylthiocarbamide locus (PTC)Iran: tricontinental nexus for Y-chromosome driven migrationPossible localization of Gc-System on chromosome 4. Loss of long arm 4 material associated with father-child incompatibility within the Gc-SystemGene differentiation among the Dhangar caste-cluster of Maharashtra, IndiaStudy of HLA antigens in patients with osteosarcomaFurther data on mitochondrial malic enzyme in manHpaII polymerase chain reaction restriction fragment length polymorphism in the human CD19 gene on 16p11Stomach aldehyde dehydrogenase: report of a new locusLinkage relations of the loci for Kell and phenylthiocarbamide taste sensitivityFinger patterns and ridge counts of patients with Klinefelter's syndrome (47, XXY) among the JapanesePopulation genetics of wild-type CAG repeats in the Machado-Joseph disease gene in PortugalWhat is the significance of a significant TDT?The TDT is a statistically valid test: comments on Wittkowski and LiuStudies on the properties and tissue distribution of the isozymes of guanylate kinase in manPhosphoglucomutase (PGM2) variants in Trio Indians from Surinam.Fine mapping of the human biotinidase gene and haplotype analysis of five common mutations.Genetics of acheiropodia (the handless and footless families of Brazil). IX. Genetic counseling.An alternative foundation for the planning and evaluation of linkage analysis. I. Decoupling "error probabilities" from "measures of evidence".Variance components linkage analysis with repeated measurementsIncreasing genotype-phenotype model determinism: application to bivariate reading/language traits and epistatic interactions in language-impaired families.Review and evaluation of methods correcting for population stratification with a focus on underlying statistical principlesThe robustness of generalized estimating equations for association tests in extended family data.Could inbred cases identified in GWAS data succeed in detecting rare recessive variants where affected sib-pairs have failed?
P1433
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P1433
description
journal
@en
revista científica
@es
rivista scientifica
@it
vědecký časopis
@cs
wetenschappelijk tijdschrift van Karger Publishers
@nl
wissenschaftliche Fachzeitschrift
@de
مجلة
@ar
name
Human Heredity
@ast
Human Heredity
@da
Human Heredity
@en
Human Heredity
@es
Human Heredity
@fi
Human Heredity
@fr
Human Heredity
@it
Human Heredity
@nb
Human Heredity
@nl
Human Heredity
@nn
type
label
Human Heredity
@ast
Human Heredity
@da
Human Heredity
@en
Human Heredity
@es
Human Heredity
@fi
Human Heredity
@fr
Human Heredity
@it
Human Heredity
@nb
Human Heredity
@nl
Human Heredity
@nn
prefLabel
Human Heredity
@ast
Human Heredity
@da
Human Heredity
@en
Human Heredity
@es
Human Heredity
@fi
Human Heredity
@fr
Human Heredity
@it
Human Heredity
@nb
Human Heredity
@nl
Human Heredity
@nn
P3181
P1055
P1156
P1277
P1476
Human Heredity: international journal of human and medical genetics
@en