scholarly article | Q13442814 |
P2093 | author name string | J. B. Clegg | |
A. J. Boyce | |||
R. M. Harding | |||
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Population bottlenecks in Polynesia revealed by minisatellites | Q56834229 | ||
Victims or perpetrators of DNA turnover? | Q59001959 | ||
Evolutionary origin and diversification of the mammalian CD1 antigen genes | Q67691457 | ||
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Analysis of somatic mutations at human minisatellite loci in tumors and cell lines | Q69599591 | ||
A sequence in M13 phage detects hypervariable minisatellites in human and animal DNA | Q69893809 | ||
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Hypervariable 'minisatellite' regions in human DNA. | Q34192489 | ||
A GGCAGG motif in minisatellites affecting their germline instability | Q34942523 | ||
New approach for isolation of VNTR markers. | Q35248153 | ||
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Molecular characterisation of a hypervariable region downstream of the human alpha-globin gene cluster | Q36425658 | ||
Chromosomal context dependence of a eukaryotic recombinational hot spot | Q36765427 | ||
Population genetics of multigene families that are dispersed into two or more chromosomes | Q37616528 | ||
Centromeres of mammalian chromosomes | Q37793925 | ||
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Minisatellite repeat coding as a digital approach to DNA typing | Q39252911 | ||
The evolution of multigene families: human haptoglobin genes | Q39461625 | ||
Detection of a novel minisatellite-specific DNA-binding protein | Q40530236 | ||
The efficiency of multilocus DNA fingerprint probes for individualization and establishment of family relationships, determined from extensive casework | Q40561735 | ||
Minisatellite allele diversification: the origin of rare alleles at the HRAS1 locus. | Q40583879 | ||
Allele frequency distribution of two highly polymorphic DNA sequences in three ethnic groups and its application to the determination of paternity. | Q40593097 | ||
Unequal crossingover between homologous chromosomes is not the major mechanism involved in the generation of new alleles at VNTR loci | Q41277519 | ||
Patterns of intra- and interarray sequence variation in alpha satellite from the human X chromosome: evidence for short-range homogenization of tandemly repeated DNA sequences | Q41282457 | ||
Molecular characterization of a spontaneously generated new allele at a VNTR locus: no exchange of flanking DNA sequence | Q41418826 | ||
Persistence of tandem arrays: implications for satellite and simple-sequence DNAs. | Q42028717 | ||
Transposition, amplification, and divergence in the origin of the DNF15 loci, a polymorphic repetitive sequence family on chromosomes 1 and 3. | Q47358097 | ||
A novel human DNA polymorphism resulting from transfer of DNA from chromosome 6 to chromosome 16. | Q48265639 | ||
Characterization of a highly unstable mouse minisatellite locus: evidence for somatic mutation during early development | Q48283386 | ||
Structure and evolution of the horse zeta globin locus | Q48329430 | ||
Mathematical models for the evolution of multigene families by unequal crossing over. | Q52817504 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | evolution | Q1063 |
genetic recombination | Q211675 | ||
repetitive DNA | Q424473 | ||
genetic model | Q67149661 | ||
P304 | page(s) | 847-859 | |
P577 | publication date | 1992-11-01 | |
P1433 | published in | Genetics | Q3100575 |
P1476 | title | The evolution of tandemly repetitive DNA: recombination rules | |
P478 | volume | 132 |
Q42190786 | A computer simulation study of VNTR population genetics: constrained recombination rules out the infinite alleles model. |
Q81153313 | A new diagnostic SSR marker for selection of the Rym4/Rym5 locus in barley breeding |
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Q91800201 | Defects in the GINS complex increase the instability of repetitive sequences via a recombination-dependent mechanism |
Q36186205 | Genetic diversity and mating type distribution of Tuber melanosporum and their significance to truffle cultivation in artificially planted truffieres in Australia. |
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Q92072806 | Recurrent gene co-amplification on Drosophila X and Y chromosomes |
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