Lista de obras -

Analysis of large mutations in BARD1 in patients with breast and/or ovarian cancer: the Polish population as an example

artículo científico publicado en 2015

BRCA1 and BRCA2 mutation analysis in breast-ovarian cancer families from northeastern Poland

artículo científico publicado en 2003

BRCA1 and BRCA2 point mutations and large rearrangements in breast and ovarian cancer families in Northern Poland

scientific article published on 01 January 2008

Cancer predisposing BARD1 mutations affect exon skipping and are associated with overexpression of specific BARD1 isoforms

artículo científico publicado en 2015

Cancer predisposing BARD1 mutations in breast-ovarian cancer families

scientific article published on 23 February 2011

Cytogenetic analysis and clinical significance of chromosome 7 aberrations in acute leukaemia

scientific article published on 01 January 2003

Frontometaphyseal dysplasia: Mutations inFLNA and phenotypic diversity

artículo científico publicado en 2006

Germline MSH2 and MLH1 mutational spectrum including large rearrangements in HNPCC families from Poland (update study)

artículo científico publicado en 2005

Germline NBS1 mutations in families with aggregation of Breast and/or ovarian cancer from north-east Poland

artículo científico publicado en 2007

HER2 Amplification Has no Prognostic Value in Sporadic and Hereditary Ovarian Tumours

artículo científico publicado en 2006

Hereditary ovarian cancer in Poland.

artículo científico publicado en 2003

High frequency of BRCA1/2 germline mutations in consecutive ovarian cancer patients in Poland

scientific article published on 07 November 2007

Limited significance of family history for presence of BRCA1 gene mutation in Polish breast and ovarian cancer cases

artículo científico publicado en 2012

Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor

artículo científico publicado en 2005

Microdeletion of target sites for insulator protein CTCF in a chromosome 11p15 imprinting center in Beckwith-Wiedemann syndrome and Wilms' tumor

artículo científico publicado en 2005

Mutational analysis of BRCA1/2 in a group of 134 consecutive ovarian cancer patients. Novel and recurrent BRCA1/2 alterations detected by next generation sequencing

artículo científico publicado en 2014

Mutations spectrum in hereditary disorders predisposing to occurrence of intestine polyposis in Poland.

artículo científico publicado en 2012

Partial trisomy of distal 5q and partial monosomy of Xp as a result of mating between two translocation carriers: a female with a balanced translocation t(X;5)(p11;q31) and a male with a der(13;14)(q10;q10)—a case report and a family study

scientific article published on 01 July 2002

Prevalence and clinical correlations of BRCA1/BRCA2 unclassified variant carriers among unselected primary ovarian cancer cases - preliminary report

scientific article published on 01 January 2005

Prevalence of the most frequent BRCA1 mutations in Polish population

artículo científico publicado en 2011

Spectrum and Prevalence of Pathogenic Variants in Ovarian Cancer Susceptibility Genes in a Group of 333 Patients

article

Lista de obras de

Analysis of large mutations in BARD1 in patients with breast and/or ovarian cancer: the Polish population as an example

BRCA1 and BRCA2 mutation analysis in breast-ovarian cancer families from northeastern Poland

BRCA1 and BRCA2 point mutations and large rearrangements in breast and ovarian cancer families in Northern Poland

Cancer predisposing BARD1 mutations affect exon skipping and are associated with overexpression of specific BARD1 isoforms

Cancer predisposing BARD1 mutations in breast-ovarian cancer families

Cytogenetic analysis and clinical significance of chromosome 7 aberrations in acute leukaemia

Frontometaphyseal dysplasia: Mutations inFLNA and phenotypic diversity

Germline MSH2 and MLH1 mutational spectrum including large rearrangements in HNPCC families from Poland (update study)

Germline NBS1 mutations in families with aggregation of Breast and/or ovarian cancer from north-east Poland

HER2 Amplification Has no Prognostic Value in Sporadic and Hereditary Ovarian Tumours

Hereditary ovarian cancer in Poland.

High frequency of BRCA1/2 germline mutations in consecutive ovarian cancer patients in Poland

Limited significance of family history for presence of BRCA1 gene mutation in Polish breast and ovarian cancer cases

Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor

Microdeletion of target sites for insulator protein CTCF in a chromosome 11p15 imprinting center in Beckwith-Wiedemann syndrome and Wilms' tumor

Mutational analysis of BRCA1/2 in a group of 134 consecutive ovarian cancer patients. Novel and recurrent BRCA1/2 alterations detected by next generation sequencing

Mutations spectrum in hereditary disorders predisposing to occurrence of intestine polyposis in Poland.

Partial trisomy of distal 5q and partial monosomy of Xp as a result of mating between two translocation carriers: a female with a balanced translocation t(X;5)(p11;q31) and a male with a der(13;14)(q10;q10)—a case report and a family study

Prevalence and clinical correlations of BRCA1/BRCA2 unclassified variant carriers among unselected primary ovarian cancer cases - preliminary report

Prevalence of the most frequent BRCA1 mutations in Polish population

Spectrum and Prevalence of Pathogenic Variants in Ovarian Cancer Susceptibility Genes in a Group of 333 Patients