Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeat (Q28304011)

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1 November 2019

title

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

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1 November 2019

2

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Denis Le Paslier

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1 November 2019

author name string

S Yu

1

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1 November 2019

D Hewett

3

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L Hobson

4

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E Baker

5

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H J Eyre

6

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N Lapsys

7

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N A Doggett

9

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G R Sutherland

10

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R I Richards

11

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language of work or name

English

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publication date

1 February 1997

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1 November 2019

volume

88

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issue

3

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1 November 2019

page(s)

367-374

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Basic local alignment search tool

1 November 2019

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Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus

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Fragile chromosome 16(q22) cause a balanced translocation at the same point

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Intergenerational instability of the CAG repeat of the gene for Machado-Joseph disease (MJD1) is affected by the genotype of the normal chromosome: implications for the molecular mechanisms of the instability of the CAG repeat

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Absence of chromosome fragility at 19q13.3 in patients with myotonic dystrophy

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Complex gene conversion events in germline mutation at human minisatellites

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Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2

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The minisatellite in the diabetes susceptibility locus IDDM2 regulates insulin transcription.

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

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Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n

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An association between the risk of cancer and mutations in the HRAS1 minisatellite locus.

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Growing triplet repeats

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Minisatellite mutation rate variation associated with a flanking DNA sequence polymorphism

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

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Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

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

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Reduction in size of the myotonic dystrophy trinucleotide repeat mutation during transmission

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Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE

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

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Dynamic mutations: a new class of mutations causing human disease

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FRA3B extends over a broad region and contains a spontaneous HPV16 integration site: direct evidence for the coincidence of viral integration sites and fragile sites

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Identifiers

DOI

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1 November 2019

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