M. Kędzior

Application of array comparative genomic hybridization in 256 patients with developmental delay or intellectual disability

P. Stankiewicz, C. Shaw, E. Obersztyn, 2013, Journal of Applied Genetics.

A placental trisomy 2 detected by NIPT evolved in a fetal small Supernumerary Marker Chromosome (sSMC)

J. Vermeesch, E. Obersztyn, A. Kucińska-Chahwan, 2020, Molecular cytogenetics.

[Cell phenotype determines PAI-1 antiproliferative effect - suppressed proliferation of the lung cancer but not prostate cancer cells].

E. Skrzypczak‐Jankun, J. Jankun, J. Chorostowska-Wynimko, 2010, Pneumonologia i alergologia polska.

phenotype determines PAI-1 antiproliferative effect — suppressed proliferation of the lung cancer but not prostate cancer cells

E. Skrzypczak‐Jankun, J. Jankun, J. Chorostowska-Wynimko, 2010 .

Differential regulation of endothelial cells proliferative and proangiogenic activity by sera from patients with lower limb ischemia

R. Proczka, J. Chorostowska-Wynimko, M. Kędzior, 2009 .

Application of array comparative genomic hybridization in 102 patients with epilepsy and additional neurodevelopmental disorders

Anna Gambin, Chad A Shaw, Tomasz Gambin, 2012, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Cytogenomic Evaluation of Children with Congenital Anomalies: Critical Implications for Diagnostic Testing and Genetic Counseling.

U. Demkow, M. Radkowski, M. Kędzior, 2016, Advances in experimental medicine and biology.

Application of array comparative genomic hybridization in 256 patients with developmental delay or intellectual disability

P. Stankiewicz, C. Shaw, E. Obersztyn, 2013, Journal of Applied Genetics.

Molecular and clinical characterization of new patient with 1,08 Mb deletion in 10p15.3 region

B. Nowakowska, M. Kędzior, J. Bernaciak, 2017, Molecular Cytogenetics.

Comparative Genomic Hybridization to Microarrays in Fetuses with High-Risk Prenatal Indications: Polish Experience with 7400 Pregnancies

E. Obersztyn, B. Wiśniowiecka-Kowalnik, M. Smyk, 2022, Genes.

Prenatal Diagnosis by Array Comparative Genomic Hybridization in Fetuses with Cardiac Abnormalities

E. Obersztyn, A. Barczyk, B. Wiśniowiecka-Kowalnik, 2021, Genes.

[Role of immune system in the pathomechanism of obstructive sleep apnea].

J. Chorostowska-Wynimko, M. Kędzior, 2008, Pneumonologia i Alergologia Polska.

Molecular and clinical characterization of new patient with 1,08 Mb deletion in 10p15.3 region

B. Nowakowska, M. Kędzior, J. Bernaciak, 2017, Molecular Cytogenetics.