(Q48469722)

11 February 2018

title

High incidence of familial breast cancer segregates with constitutional t(11;22)(q23;q11). (English)

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11 February 2018

author name string

Ilse Wieland

1

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11 February 2018

Petra Muschke

2

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11 February 2018

Marianne Volleth

3

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11 February 2018

Albrecht Röpke

4

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11 February 2018

Antje-Friederike Pelz

5

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11 February 2018

Markus Stumm

6

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11 February 2018

Peter Wieacker

7

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11 February 2018

publication date

1 October 2006

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11 February 2018

Genes, Chromosomes and Cancer

published in

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11 February 2018

volume

45

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11 February 2018

issue

10

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11 February 2018

page(s)

945-949

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11 February 2018

Loss of heterozygosity analysis on chromosome 5p defines 5p13-12 as the critical region involved in tumor progression of bladder carcinomas

cites work

1 reference

7 January 2021

Familial breast cancer: collaborative reanalysis of individual data from 52 epidemiological studies including 58,209 women with breast cancer and 101,986 women without the disease

1 reference

7 January 2021

Genes other than BRCA1 and BRCA2 involved in breast cancer susceptibility

1 reference

7 January 2021

Chromosome 22 tiling-path array-CGH analysis identifies germ-line- and tumor-specific aberrations in patients with glioblastoma multiforme.

1 reference

7 January 2021

Understanding breast cancer risk -- where do we stand in 2005?

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7 January 2021

AT-rich palindromes mediate the constitutional t(11;22) translocation.

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7 January 2021

A common breakpoint on 11q23 in carriers of the constitutional t(11;22) translocation

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7 January 2021

The most frequent constitutional translocation in humans, the t(11;22)(q23;q11) is due to a highly specific alu-mediated recombination

1 reference

7 January 2021

The 11q;22q translocation: a collaborative study of 20 new cases and analysis of 110 families

1 reference

7 January 2021

Comparative genomic hybridisation of ductal carcinoma in situ of the breast: identification of regions of DNA amplification and deletion in common with invasive breast carcinoma

1 reference

7 January 2021

A unique case of der(11)t(11;22),-22 arising from 3:1 segregation of a maternal t(11;22) in a family with co-segregation of the translocation and breast cancer

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7 January 2021

Long AT-rich palindromes and the constitutional t(11;22) breakpoint

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7 January 2021

Unexpectedly high rate of de novo constitutional t(11;22) translocations in sperm from normal males

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7 January 2021

Tightly clustered 11q23 and 22q11 breakpoints permit PCR-based detection of the recurrent constitutional t(11;22).

1 reference

7 January 2021

The BCSC-1 locus at chromosome 11q23-q24 is a candidate tumor suppressor gene

1 reference

7 January 2021

Characterization of Familial Non-BRCA1/2 Breast Tumors by Loss of Heterozygosity and Immunophenotyping

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7 January 2021

Promoter CpG hypermethylation and downregulation of DICE1 expression in prostate cancer

1 reference

7 January 2021

Clustered 11q23 and 22q11 breakpoints and 3:1 meiotic malsegregation in multiple unrelated t(11;22) families

1 reference

7 January 2021

Fine mapping of the constitutional translocation t(11;22)(q23;q11).

1 reference

7 January 2021

Site-specific reciprocal translocation, t(11;22) (q23;q11), in several unrelated families with 3:1 meiotic disjunction

1 reference

7 January 2021

Identifiers

DOI

10.1002/GCC.20358

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11 February 2018

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11 February 2018