(Q34067341)

30 July 2017

1 reference

title

Masquerading repeats: paralogous pitfalls of the human genome (English)

1 reference

30 July 2017

Eichler EE

1

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30 July 2017

1 August 1998

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30 July 2017

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30 July 2017

8

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30 July 2017

758-762

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30 July 2017

8

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Comparative mapping of DNA probes derived from the V kappa immunoglobulin gene regions on human and great ape chromosomes by fluorescence in situ hybridization.

30 July 2017

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

In-frame deletion of von Willebrand factor A domains in a dominant type of von Willebrand disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

Structural features of transposed human VK genes and implications for the mechanism of their transpositions

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

A physical map of human chromosome 7: an integrated YAC contig map with average STS spacing of 79 kb.

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

Repeated sequences in DNA. Hundreds of thousands of copies of DNA sequences have been incorporated into the genomes of higher organisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

Inherited interstitial duplications of proximal 15q: genotype-phenotype correlations

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

A putative gene family in 15q11-13 and 16p11.2: possible implications for Prader-Willi and Angelman syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

Inter- and intrachromosomal rearrangements are both involved in the origin of 15q11-q13 deletions in Prader-Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

Duplication of a gene-rich cluster between 16p11.1 and Xq28: a novel pericentromeric-directed mechanism for paralogous genome evolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

Interchromosomal duplications of the adrenoleukodystrophy locus: a phenomenon of pericentromeric plasticity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

The immunoglobulin kappa locus of primates

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

Immunoglobulin lambda light chain orphons on human chromosome 8q11.2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

Low-copy-number repeat sequences flank the DiGeorge/velo-cardio-facial syndrome loci at 22q11.

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

Refined molecular characterization of the breakpoints in small inv dup(15) chromosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

The dawn of the post-genome era, seen from the ocean front

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

A third neurofibromatosis type 1 (NF1) pseudogene at chromosome 15q11.2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

Long-range mapping and construction of a YAC contig within the cat eye syndrome critical region

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

Formation of large deletions by illegitimate recombination in the HPRT gene of primary human fibroblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

Assignment of the human aggrecan gene (AGC1) to 15q26 using fluorescence in situ hybridization analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

Emergence and scattering of multiple neurofibromatosis (NF1)-related sequences during hominoid evolution suggest a process of pericentromeric interchromosomal transposition.

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

A recombination hotspot responsible for two inherited peripheral neuropathies is located near a mariner transposon-like element.

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

Distribution of olfactory receptor genes in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

Human immunoglobulin VH and D segments on chromosomes 15q11.2 and 16p11.2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

Members of the olfactory receptor gene family are contained in large blocks of DNA duplicated polymorphically near the ends of human chromosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

A new strategy for genome sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

Shotgun sequencing of the human genome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

A novel human DNA polymorphism resulting from transfer of DNA from chromosome 6 to chromosome 16.

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

The immunoglobulin kappa locus-or-what has been learned from looking closely at one-tenth of a percent of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

Fluorescence in situ hybridization analysis of keratinocyte growth factor gene amplification and dispersion in evolution of great apes and humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.8.8.758

21 January 2018

Identifiers

DOI

10.1101/GR.8.8.758

1 reference

30 July 2017

1 reference

PubMed ID

9724321