Identification of a novel splice-site mutation of the BRCA1 gene in two breast cancer families: Screening reveals low frequency in Icelandic breast cancer patients-Reference-Cited by-同舟云学术

Identification of a novel splice-site mutation of the BRCA1 gene in two breast cancer families: Screening reveals low frequency in Icelandic breast cancer patients

Published:1998 Issue:S1 Volume:11 Page:S195-S197
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Bergthorsson Jon Thor,Jonasdottir Adalbjorg,Johannesdottir Gudrun,Arason Adalgeir,Egilsson Valgardur,Gayther Simon,Borg Ake,Hakanson Sara,Ingvarsson Sigurdur,Barkardottir Rosa Bjork

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference9 articles.

1. Linkage analyses of chromosome 17q markers and breast-ovarian cancer in Icelandic families, and possible relationship to prostatic cancer;Arason;Am J Hum Genet,1993

2. Chromosome 17q-linkage seems to be infrequent in Icelandic families at risk of breast cancer;Barkardottir;Acta Oncol,1995

3. Genetic analysis of cancer in the cancer and steroid hormone study;Claus;Am J Hum Genet,1991

4. Genetic linkage analysis in familial breast and ovarian cancer: Results from 214 families;Easton;Am J Hum Genet,1993

5. Frequent occurrence of BRCA2 linkage in Icelandic breast cancer families and segregation of a common BRCA2 haplotype;Gudmundsson;Am J Hum Genet,1996

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