The BRCA1 exon 13 duplication in the Swedish population (Q57741875)

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English	The BRCA1 exon 13 duplication in the Swedish population	No description defined

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instance of

scholarly article

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title

The BRCA1 exon 13 duplication in the Swedish population (English)

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author

Margareta Nordling

object named as

Margareta Nordling

series ordinal

6

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Kristina Lagerstedt Robinson

object named as

Kristina Lagerstedt

series ordinal

3

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Sylvie Mazoyer

object named as

Sylvie Mazoyer

series ordinal

5

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Annika Lindblom

series ordinal

8

object named as

Annika Lindblom

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author name string

Barbara Kremeyer

series ordinal

1

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Maria Soller

series ordinal

2

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Paula Maguire

series ordinal

4

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Jan Wahlström

series ordinal

7

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publication date

June 2005

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published in

Familial Cancer

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volume

4

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issue

2

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page(s)

191-194

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cites work

Germline BRCA1 promoter deletions in UK and Australian familial breast cancer patients: Identification of a novel deletion consistent with BRCA1:psiBRCA1 recombination.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15951973

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening for germ-line rearrangements and regulatory mutations in BRCA1 led to the identification of four new deletions

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15951973

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid detection of novel BRCA1 rearrangements in high-risk breast-ovarian cancer families using multiplex PCR of short fluorescent fragments

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15951973

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An Alu-mediated 7.1 kb deletion of BRCA1 exons 8 and 9 in breast and ovarian cancer families that results in alternative splicing of exon 10

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15951973

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Computer programs for multilocus haplotyping of general pedigrees.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15951973

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening for genomic rearrangements in families with breast and ovarian cancer identifies BRCA1 mutations previously missed by conformation-sensitive gel electrophoresis or sequencing

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15951973

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An Alu-mediated 6-kb duplication in the BRCA1 gene: a new founder mutation?

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15951973

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a 14 kb deletion involving the promoter region of BRCA1 in a breast cancer family

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15951973

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BRCA2 germline mutations in Swedish breast cancer families.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15951973

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15951973

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterisation of a 161 kb deletion extending from the NBR1 to the BRCA1 genes in a French breast-ovarian cancer family

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15951973

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complex germline rearrangement of BRCA1 associated with breast and ovarian cancer

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15951973

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic rearrangements account for more than one-third of the BRCA1 mutations in northern Italian breast/ovarian cancer families

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15951973

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A 1-kb Alu-mediated germ-line deletion removing BRCA1 exon 17

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15951973

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BRCA1 screening in patients with a family history of breast or ovarian cancer

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15951973

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15951973

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The exon 13 duplication in the BRCA1 gene is a founder mutation present in geographically diverse populations. The BRCA1 Exon 13 Duplication Screening Group

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15951973

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a large rearrangement of the BRCA1 gene using colour bar code on combed DNA in an American breast/ovarian cancer family previously studied by direct sequencing

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15951973

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Significant contribution of large BRCA1 gene rearrangements in 120 French breast and ovarian cancer families

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15951973

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S10689-004-7023-2

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PubMed publication ID

15951973

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