(Q47981696)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9624249%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

title

Chromosome imbalance at the 3p14 region in human breast tumours: high frequency in patients with inherited predisposition due to BRCA2 (English)

1 reference

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12 November 2019

1

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12 November 2019

Sigurður Ingvarsson

6

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12 November 2019

author name string

J Johannsdottir

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9624249%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

A Jonasdottir

3

1 reference

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12 November 2019

G Eiriksdottir

4

1 reference

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12 November 2019

V Egilsson

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9624249%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

R B Barkardottir

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9624249%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

A Arason

8

1 reference

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12 November 2019

publication date

1 January 1998

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European Journal of Cancer

12 November 2019

published in

1 reference

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12 November 2019

volume

34

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12 November 2019

page(s)

142-147

1 reference

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12 November 2019

issue

1

1 reference

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Consistent chromosome 3p deletion and loss of heterozygosity in renal cell carcinoma

12 November 2019

cites work

1 reference

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7 January 2021

Chromosome abnormalities in benign hyperproliferative disorders of epithelial and stromal breast tissue

1 reference

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7 January 2021

Interstitial deletion of the short arm of chromosome 3 as a primary chromosome abnormality in carcinomas of the breast

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7 January 2021

Population cytogenetics of aphidicolin-induced fragile sites

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7 January 2021

Precise localization of aphidicolin-induced breakpoints on the short arm of human chromosome 3

1 reference

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7 January 2021

Hereditary Renal-Cell Carcinoma Associated with a Chromosomal Translocation

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900339-0

7 January 2021

Fhit, a putative tumor suppressor in humans, is a dinucleoside 5',5"'-P1,P3-triphosphate hydrolase

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900339-0

7 January 2021

The FHIT gene 3p14.2 is abnormal in lung cancer.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900339-0

7 January 2021

Receptor protein-tyrosine phosphatase gamma is a candidate tumor suppressor gene at human chromosome region 3p21

1 reference

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7 January 2021

Mapping of chromosome-3 alterations in human breast-cancer using microsatellite PCR markers - correlation with clinical-variables

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7 January 2021

Linkage analysis and allelic imbalance in human breast cancer kindreds using microsatellite markers from the short arm of chromosome 3

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7 January 2021

The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds

1 reference

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7 January 2021

A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes

1 reference

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7 January 2021

The use of loss of constitutional heterozygosity data to ascertain the location of predisposing genes in cancer families

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900339-0

7 January 2021

Allele losses in the region 17q12-21 in familial breast and ovarian cancer involve the wild-type chromosome

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900339-0

7 January 2021

Chromosome 17q-linkage seems to be infrequent in Icelandic families at risk of breast cancer

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900339-0

7 January 2021

Detection and mapping of amplified DNA sequences in breast cancer by comparative genomic hybridization

1 reference

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7 January 2021

Expression of aphidicolin-induced fragile sites in lymphocytes of patients with breast cancer

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900339-0

7 January 2021

Expressivity of a common fragile site, fra(3)(p14.2), in patients with cancer and other diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900339-0

7 January 2021

Comparison of p53 gene abnormalities in bilateral and unilateral breast cancer.

1 reference

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7 January 2021

Chromosome 3p14 homozygous deletions and sequence analysis of FRA3B.

1 reference

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7 January 2021

BRCA1 mutations in primary breast and ovarian carcinomas.

1 reference

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7 January 2021

Mutation analysis in the BRCA2 gene in primary breast cancers

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900339-0

7 January 2021

Low incidence of BRCA2 mutations in breast carcinoma and other cancers

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900339-0

7 January 2021

The enigma of common fragile sites

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900339-0

7 January 2021

Association of BRCA1 with Rad51 in mitotic and meiotic cells

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900339-0

7 January 2021

Embryonic lethality and radiation hypersensitivity mediated by Rad51 in mice lacking Brca2

1 reference

https://api.crossref.org/works/10.1016%2FS0959-8049%2897%2900339-0

7 January 2021

10.1016/S0959-8049(97)00339-0

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9624249%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

1 reference