(Q41061223)

English

Fish mapping of YAC clones at human chromosomal band 7q31.2: identification of YACS spanning FRA7G within the common region of LOH in breast and prostate cancer

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

26 September 2017

Fish mapping of YAC clones at human chromosomal band 7q31.2: identification of YACS spanning FRA7G within the common region of LOH in breast and prostate cancer (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 September 2017

prostate cancer

1 reference

based on heuristic

inferred from title

author name string

Huang H

1

1 reference

Europe PubMed Central

PubMed publication ID

26 September 2017

Qian C

2

1 reference

Europe PubMed Central

PubMed publication ID

26 September 2017

Jenkins RB

3

1 reference

Europe PubMed Central

PubMed publication ID

26 September 2017

Smith DI

4

1 reference

Europe PubMed Central

PubMed publication ID

26 September 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

1 February 1998

1 reference

Europe PubMed Central

PubMed publication ID

26 September 2017

Genes, Chromosomes and Cancer

1 reference

Europe PubMed Central

PubMed publication ID

26 September 2017

21

1 reference

Europe PubMed Central

PubMed publication ID

26 September 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

26 September 2017

152-159

1 reference

Europe PubMed Central

PubMed publication ID

26 September 2017

Mapping the whole human genome by fingerprinting yeast artificial chromosomes

1 reference

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21 January 2018

Report of the Committee on Chromosome Rearrangements in Neoplasia and on Fragile Sites

1 reference

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21 January 2018

Integrated YAC contig containing the 3p14.2 hereditary renal carcinoma 3;8 translocation breakpoint and the fragile site FRA3B.

1 reference

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21 January 2018

Chromosome 3p14 homozygous deletions and sequence analysis of FRA3B.

1 reference

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21 January 2018

YAC mapping by FISH using Alu-PCR-generated probes

1 reference

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21 January 2018

Hereditary Renal-Cell Carcinoma Associated with a Chromosomal Translocation

1 reference

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21 January 2018

Expression of fragile sites triggers intrachromosomal mammalian gene amplification and sets boundaries to early amplicons

1 reference

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21 January 2018

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

1 reference

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21 January 2018

DNA polymerase alpha inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes

1 reference

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21 January 2018

Systematic generation of sequence-tagged sites for physical mapping of human chromosomes: Application to the mapping of human chromosome 7 using yeast artificial chromosomes

1 reference

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21 January 2018

Sister chromatid exchanges are preferentially induced at expressed and nonexpressed common fragile sites

1 reference

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21 January 2018

Biochemical and genetic analysis of the Chinese hamster mutants irs1 and irs2 and their comparison to cultured ataxia telangiectasia cells

1 reference

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21 January 2018

Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation.

1 reference

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21 January 2018

Frequent loss of heterozygosity in the region of the D7S523 locus in advanced ovarian cancer

1 reference

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21 January 2018

Cell type-dependent difference in the distribution and frequency of excess thymidine-induced common fragile sites: T lymphocytes and skin fibroblasts

1 reference

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21 January 2018

"PCR-karyotype" of human chromosomes in somatic cell hybrids

1 reference

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21 January 2018

Implications of FRA16A structure for the mechanism of chromosomal fragile site genesis

1 reference

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21 January 2018

Alu polymerase chain reaction: a method for rapid isolation of human-specific sequences from complex DNA sources

1 reference

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21 January 2018

The FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated t(3;8) breakpoint, is abnormal in digestive tract cancers

1 reference

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21 January 2018

Absence of expression of the FMR-1 gene in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199802%2921%3A2%3C152%3A%3AAID-GCC11%3E3.0.CO%3B2-T

21 January 2018

The cloning of FRAXF: trinucleotide repeat expansion and methylation at a third fragile site in distal Xqter.

1 reference

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21 January 2018

Report of the committee on cytogenetic markers

1 reference

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21 January 2018

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

1 reference

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21 January 2018

Multicolor FISH mapping of YAC clones in 3p14 and identification of a YAC spanning both FRA3B and the t(3;8) associated with hereditary renal cell carcinoma

1 reference

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21 January 2018

Fragile X genotype characterized by an unstable region of DNA.

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21 January 2018

Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeat

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21 January 2018

Constitutive fragile sites and cancer.

1 reference

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21 January 2018

(C-A)n microsatellite repeat D7S522 is the most commonly deleted region in human primary breast cancer

1 reference

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21 January 2018

Identifiers

10.1002/(SICI)1098-2264(199802)21:2<152::AID-GCC11>3.0.CO;2-T

1 reference

Europe PubMed Central

PubMed publication ID

26 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 September 2017

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