Mutation analysis of BRCA1 and BRCA2 genes in Iranian high risk breast cancer families (Q81787605)

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12 January 2020

title

Mutation analysis of BRCA1 and BRCA2 genes in Iranian high risk breast cancer families (English)

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12 January 2020

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8

Stefan Mundlos

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12 January 2020

author name string

Andrea Pietschmann

1

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12 January 2020

Parvin Mehdipour

2

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12 January 2020

Parvin Mehdipour

3

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12 January 2020

Morteza Atri

4

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12 January 2020

Wera Hofmann

5

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12 January 2020

S Said Hosseini-Asl

6

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12 January 2020

Siegfried Scherneck

7

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12 January 2020

Hartmut Peters

9

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publication date

26 May 2005

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Journal of Cancer Research and Clinical Oncology

12 January 2020

published in

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volume

131

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issue

8

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page(s)

552-558

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https://scigraph.springernature.com/pub.10.1007/s00432-005-0678-8

12 January 2020

exact match

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cites work

The Iranian Human Mutation Gene Bank: a data and sample resource for worldwide collaborative genetics research.

1 reference

12 December 2020

Polymorphisms in DNA repair genes and associations with cancer risk

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12 December 2020

Variation in cancer risks, by mutation position, in BRCA2 mutation carriers

1 reference

12 December 2020

BRCA1 sequence analysis in women at high risk for susceptibility mutations. Risk factor analysis and implications for genetic testing.

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12 December 2020

Founder populations and their uses for breast cancer genetics

1 reference

12 December 2020

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

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12 December 2020

Analysis of BRCA1 and BRCA2 mutations in an Iranian family with hereditary breast and ovarian cancer syndrome

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12 December 2020

Laddering through pedigrees: family history of malignancies in primary breast cancer patients

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12 December 2020

Detection of large rearrangements of exons 13 and 22 in the BRCA1 gene in German families

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12 December 2020

A common variant in BRCA2 is associated with both breast cancer risk and prenatal viability

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12 December 2020

Nomenclature for the description of human sequence variations.

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12 December 2020

Germline BRCA1 mutations in Iranian women with breast cancer.

1 reference

12 December 2020

Novel mutations in the BRCA1 and BRCA2 genes in Iranian women with early-onset breast cancer

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12 December 2020

Analysis of BRCA1 and BRCA2 genes in Spanish breast/ovarian cancer patients: a high proportion of mutations unique to Spain and evidence of founder effects

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12 December 2020

Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2

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12 December 2020

Hereditary breast and ovarian cancer in Asia: genetic epidemiology of BRCA1 and BRCA2.

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Evidence for effective suppression of recombination in the chromosome 17q21 segment spanning RNU2-BRCA1.

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12 December 2020

10.1007/S00432-005-0678-8

Identifiers

DOI

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12 January 2020

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