Refinement of a chimpanzee pericentric inversion breakpoint to a segmental duplication cluster
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B. Roe | E. Eichler | D. Locke | N. Archidiacono | D. Misceo | M. Cardone | S. Deschamps | M. Rocchi | Devin P. Locke
[1] M J White,et al. Models of speciation. New concepts suggest that the classical sympatric and allopatric models are not the only alternatives. , 1968, Science.
[2] M. King,et al. Evolution at two levels in humans and chimpanzees. , 1975, Science.
[3] J. Sawyer,et al. The striking resemblance of high-resolution G-banded chromosomes of man and chimpanzee. , 1980, Science.
[4] G Hermanson,et al. High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones. , 1990, Science.
[5] M. King. Species Evolution: The Role of Chromosome Change , 1993 .
[6] D. Ledbetter,et al. Integrated YAC contig map of the Prader-Willi/Angelman region on chromosome 15q11-q13 with average STS spacing of 35 kb. , 1998, Genome research.
[7] E. Nickerson,et al. Molecular definition of pericentric inversion breakpoints occurring during the evolution of humans and chimpanzees. , 1998, Genomics.
[8] S. Schwartz,et al. Molecular cytogenetic evidence for a common breakpoint in the largest inverted duplications of chromosome 15. , 1998, American journal of human genetics.
[9] D. Ledbetter,et al. Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13). , 1999, Human molecular genetics.
[10] D. J. Driscoll,et al. Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints. , 1999, American journal of human genetics.
[11] L. Stubbs,et al. The ancestral gene for transcribed, low-copy repeats in the Prader-Willi/Angelman region encodes a large protein implicated in protein trafficking, which is deficient in mice with neuromuscular and spermiogenic abnormalities. , 1999, Human molecular genetics.
[12] E. Eichler,et al. The mosaic structure of human pericentromeric DNA: a strategy for characterizing complex regions of the human genome. , 2000, Genome research.
[13] E. Eichler,et al. Structure of chromosomal duplicons and their role in mediating human genomic disorders. , 2000, Genome research.
[14] R. Schultz,et al. Structure of the highly conserved HERC2 gene and of multiple partially duplicated paralogs in human. , 2000, Genome research.
[15] S. Schwartz,et al. Isolation and molecular analysis of inv dup(15) and construction of a physical map of a common breakpoint in order to elucidate their mechanism of formation , 2000, Chromosoma.
[16] A. Zelenetz,et al. Cloning and characterization of a Golgin-related gene from the large-scale polymorphism linked to the PML gene. , 2000, Genomics.
[17] Xavier Estivill,et al. A Polymorphic Genomic Duplication on Human Chromosome 15 Is a Susceptibility Factor for Panic and Phobic Disorders , 2001, Cell.
[18] E. Eichler,et al. Divergent origins and concerted expansion of two segmental duplications on chromosome 16. , 2001, The Journal of heredity.
[19] Paul Richardson,et al. Human Chromosome 19 and Related Regions in Mouse: Conservative and Lineage-Specific Evolution , 2001, Science.
[20] M. Gratacós,et al. Additional complexity on human chromosome 15q: identification of a set of newly recognized duplicons (LCR15) on 15q11-q13, 15q24, and 15q26. , 2001, Genome research.
[21] P. Stankiewicz,et al. The evolutionary chromosome translocation 4;19 in Gorilla gorilla is associated with microduplication of the chromosome fragment syntenic to sequences surrounding the human proximal CMT1A-REP. , 2001, Genome research.
[22] B. Trask,et al. Segmental duplications: organization and impact within the current human genome project assembly. , 2001, Genome research.
[23] J. V. Moran,et al. Initial sequencing and analysis of the human genome. , 2001, Nature.
[24] D. Collier,et al. A 3-Mb map of a large Segmental duplication overlapping the alpha7-nicotinic acetylcholine receptor gene (CHRNA7) at human 15q13-q14. , 2002, Genomics.
[25] Mouse Genome Sequencing Consortium. Initial sequencing and comparative analysis of the mouse genome , 2002, Nature.
[26] Tom H. Pringle,et al. The human genome browser at UCSC. , 2002, Genome research.
[27] Colin N. Dewey,et al. Initial sequencing and comparative analysis of the mouse genome. , 2002 .
[28] P. Stankiewicz,et al. Molecular-evolutionary mechanisms for genomic disorders. , 2002, Current opinion in genetics & development.
[29] M. Gratacós,et al. Human chromosome 15q11-q14 regions of rearrangements contain clusters of LCR15 duplicons , 2002, European Journal of Human Genetics.
[30] M. Adams,et al. Recent Segmental Duplications in the Human Genome , 2002, Science.
[31] Matthias Platzer,et al. Molecular characterization of the pericentric inversion that causes differences between chimpanzee chromosome 19 and human chromosome 17. , 2002, American journal of human genetics.
[32] R. Verma,et al. The genomic sequence for Prader-Willi/Angelman syndromes' loci of human is apparently conserved in the great apes , 1995, Journal of Molecular Evolution.
[33] W. Willis,et al. The Origin of Man : A Chromosomal Pictorial Legacy , 2014 .