Lista de obras -

Assessment of chromosomal imbalances in CIMP-high and CIMP-low/CIMP-0 colorectal cancers

artículo científico publicado en 2012

Basal cell carcinoma of the skin: whole genome screening by comparative genome hybridization revisited.

artículo científico publicado en 2012

Cancer stem cells: the theory and perspectives in cancer therapy.

artículo científico publicado en 2008

Clinical characteristics of Polish patients with molecularly confirmed Mowat-Wilson syndrome

artículo científico publicado en 2021

DNA methylation abundantly associates with fetal alcohol spectrum disorder and its subphenotypes

artículo científico publicado en 2019

Familial distal monosomy 3p26.3-pter with trisomy 4q32.2-qter, presenting with progressive ataxia, intellectual disability, and dysmorphic features

artículo científico publicado en 2012

Fragile X syndrome in females - a familial case report and review of the literature

artículo científico publicado en 2016

Genetic testing in Poland and Ukraine: should comprehensive germline testing of BRCA1 and BRCA2 be recommended for women with breast and ovarian cancer?

scientific article published on 10 August 2020

Genetic variants in ATM, H2AFX and MRE11 genes and susceptibility to breast cancer in the polish population.

artículo científico publicado en 2018

Indices of Insulin Resistance and Dyslipidemia Are Correlated with Lymphocyte Proneness to Apoptosis in Obese or Overweight Low Birth Weight Children ⬇️

artículo científico publicado el 15 de mayo de 2013

Influence of polymorphisms in xenobiotic-metabolizing genes and DNA-repair genes on diepoxybutane-induced SCE frequency.

artículo científico publicado en 2006

May autophagy be a novel biomarker and antitumor target in colorectal cancer?

artículo científico publicado en 2016

Multiplex Ligation - dependent Probe Amplification (MLPA) as a screening test in children with developmental defects and intellectual disability of unknown etiology

artículo científico publicado el 1 de abril de 2011

Multiplex ligation-dependent probe amplification as a screening test in children with autism spectrum disorders

scientific article published on 01 January 2020

Pan-cancer analysis reveals presence of pronounced DNA methylation drift in CpG island methylator phenotype clusters

artículo científico publicado en 2017

Panhypopituitary insufficiency in a patient with clinical diagnosis of Chitayat-Hall syndrome

artículo científico publicado en 2010

Personalized medicine in oncology. New perspectives in management of gliomas.

artículo científico publicado en 2018

Phenotypic consequences of gene disruption by a balanced de novo translocation involving SLC6A1 and NAA15.

artículo científico publicado en 2018

Polymorphism in nucleotide excision repair gene XPC correlates with bleomycin-induced chromosomal aberrations

artículo científico publicado en 2007

Polymorphisms in nucleotide excision repair genes and basal cell carcinoma of the skin

artículo científico publicado en 2014

Prenatal diagnosis--principles of diagnostic procedures and genetic counseling.

scientific article published on January 2007

Rapid diagnosis of the most common fetal aneuploidies with the QF-PCR method--a study of 100 cases

artículo científico publicado en 2015

Rett syndrome. Classical form and preserved speech variant as a different phenotype effect of deletion with the same starting point in MeCP2 gene - report of 2 cases

artículo científico publicado el 1 de octubre de 2011

Single nucleotide polymorphisms in theRET gene and their correlations with Hirschsprung disease phenotype

article

The C/A polymorphism in intron 11 of the XPC gene plays a crucial role in the modulation of an individual's susceptibility to sporadic colorectal cancer

artículo científico publicado en 2011

[Perinatal palliative care performed in obstetrics and neonatology wards and hospices for children - own experience]

artículo científico publicado en 2019

[Rapid-FISH--fast and reliable method of detecting common numerical chromosomal aberrations in prenatal diagnosis]

scientific article published on 01 December 2007

Lista de obras de

Assessment of chromosomal imbalances in CIMP-high and CIMP-low/CIMP-0 colorectal cancers

Basal cell carcinoma of the skin: whole genome screening by comparative genome hybridization revisited.

Cancer stem cells: the theory and perspectives in cancer therapy.

Clinical characteristics of Polish patients with molecularly confirmed Mowat-Wilson syndrome

DNA methylation abundantly associates with fetal alcohol spectrum disorder and its subphenotypes

Familial distal monosomy 3p26.3-pter with trisomy 4q32.2-qter, presenting with progressive ataxia, intellectual disability, and dysmorphic features

Fragile X syndrome in females - a familial case report and review of the literature

Genetic testing in Poland and Ukraine: should comprehensive germline testing of BRCA1 and BRCA2 be recommended for women with breast and ovarian cancer?

Genetic variants in ATM, H2AFX and MRE11 genes and susceptibility to breast cancer in the polish population.

Indices of Insulin Resistance and Dyslipidemia Are Correlated with Lymphocyte Proneness to Apoptosis in Obese or Overweight Low Birth Weight Children ⬇️

Influence of polymorphisms in xenobiotic-metabolizing genes and DNA-repair genes on diepoxybutane-induced SCE frequency.

May autophagy be a novel biomarker and antitumor target in colorectal cancer?

Multiplex Ligation - dependent Probe Amplification (MLPA) as a screening test in children with developmental defects and intellectual disability of unknown etiology

Multiplex ligation-dependent probe amplification as a screening test in children with autism spectrum disorders

Pan-cancer analysis reveals presence of pronounced DNA methylation drift in CpG island methylator phenotype clusters

Panhypopituitary insufficiency in a patient with clinical diagnosis of Chitayat-Hall syndrome

Personalized medicine in oncology. New perspectives in management of gliomas.

Phenotypic consequences of gene disruption by a balanced de novo translocation involving SLC6A1 and NAA15.

Polymorphism in nucleotide excision repair gene XPC correlates with bleomycin-induced chromosomal aberrations

Polymorphisms in nucleotide excision repair genes and basal cell carcinoma of the skin

Prenatal diagnosis--principles of diagnostic procedures and genetic counseling.

Rapid diagnosis of the most common fetal aneuploidies with the QF-PCR method--a study of 100 cases

Rett syndrome. Classical form and preserved speech variant as a different phenotype effect of deletion with the same starting point in MeCP2 gene - report of 2 cases

Single nucleotide polymorphisms in theRET gene and their correlations with Hirschsprung disease phenotype

The C/A polymorphism in intron 11 of the XPC gene plays a crucial role in the modulation of an individual's susceptibility to sporadic colorectal cancer

[Perinatal palliative care performed in obstetrics and neonatology wards and hospices for children - own experience]

[Rapid-FISH--fast and reliable method of detecting common numerical chromosomal aberrations in prenatal diagnosis]