(Q34081489)

30 July 2017

1 reference

title

The clinical significance of fragile sites on human chromosomes (English)

1 reference

30 July 2017

Sutherland GR

1

1 reference

PubMed ID

11076037

30 July 2017

Baker E

series ordinal

2

1 reference

30 July 2017

1 September 2000

1 reference

30 July 2017

1 reference

30 July 2017

58

1 reference

30 July 2017

157-161

1 reference

30 July 2017

3

1 reference

Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome.

30 July 2017

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580301.X

Translational suppression by trinucleotide repeat expansion at FMR1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580301.X

Imprinting effect in premature ovarian failure confined to paternally inherited fragile X premutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580301.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580301.X

Constitutive fragile sites and cancer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580301.X

Cancer-specific chromosome alterations in the constitutive fragile region FRA3B.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580301.X

Aberrant transcripts of the FHIT gene are expressed in normal and leukaemic haemopoietic cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580301.X

Genes encoding human caveolin-1 and -2 are co-localized to the D7S522 locus (7q31.1), a known fragile site (FRA7G) that is frequently deleted in human cancers

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580301.X

Incidence and significance of chromosome mosaicism involving an autosomal structural abnormality diagnosed prenatally through amniocentesis: a collaborative study

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580301.X

A variant of the fra(X) syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580301.X

A new apparently folate sensitive fragile site, 5q35.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580301.X

Reproductive outcome in 3 families with a satellited chromosome 4 with review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580301.X

Fragile X premutation is a significant risk factor for premature ovarian failure: the International Collaborative POF in Fragile X study--preliminary data

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580301.X

7 January 2021

Homozygotes for FRA16B are normal

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580301.X

7 January 2021

Most Jacobsen syndrome deletion breakpoints occur distal to FRA11B

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580301.X

7 January 2021

Instability at chromosomal fragile sites

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580301.X

7 January 2021

New heritable fragile site with spontaneous expression at 1q41

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580301.X

7 January 2021

An interstitial nucleolus organizer region in the long arm of human chromosome 7: cytogenetic characterization and familial segregation

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580301.X

7 January 2021

10.1034/J.1399-0004.2000.580301.X

Identifiers

DOI

1 reference

30 July 2017

1 reference

PubMed ID

11076037