Contribution of the <it>PALB2</it> c.2323C>T [p.Q775X] Founder mutation in well-defined breast and/or ovarian cancer families and unselected ovarian cancer cases of French Canadian descent
<p>Abstract</p> <p>Background</p> <p>The <it>PALB2</it> c.2323C>T [p.Q775X] mutation has been reported in at least three breast cancer families and breast cancer cases of French Canadian descent and this has been attributed to common ancestors. The number...
Saved in:
Main Authors: | Tischkowitz Marc (Author), Sabbaghian Nelly (Author), Hamel Nancy (Author), Pouchet Carly (Author), Foulkes William D (Author), Mes-Masso (Author), Provencher Diane M (Author), Tonin Patricia N (Author) |
---|---|
Format: | Book |
Published: |
BMC,
2013-01-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
A novel germline <it>PALB2 </it>deletion in Polish breast and ovarian cancer patients
by: Cendrowski Krzysztof, et al.
Published: (2010) -
Influence of monolayer, spheroid, and tumor growth conditions on chromosome 3 gene expression in tumorigenic epithelial ovarian cancer cell lines
by: Provencher Diane M, et al.
Published: (2008) -
BMP-2 signaling in ovarian cancer and its association with poor prognosis
by: Le Page Cécile, et al.
Published: (2009) -
Haplotype analysis suggest common founders in carriers of the recurrent <it>BRCA2 </it>mutation, 3398delAAAAG, in French Canadian hereditary breast and/ovarian cancer families
by: Foulkes William D, et al.
Published: (2006) -
Prevalence of tumor BRCA1 and BRCA2 dysfunction in unselected patients with ovarian cancer
by: Roshni D. Kalachand, et al.
Published: (2020)