Ryszard Slezak
Wroclaw, DS 50368, Poland
Last Updated: 09/26/2026
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Found 26 publications
The results of CNVs analysis in patients with neurodevelopmental delay, dysmorphic features and congenital defects.
Journal: Journal of applied genetics
Published: December 18, 2025
Occurrence of Esophageal Atresia With Tracheoesophageal Fistula in Siblings From Three-Generation Family Affected by Variable Expressivity MYCN Mutation: A Case Report.
Journal: Frontiers in pediatrics
Published: September 26, 2021
Further Delineation of Phenotype and Genotype of Primary Microcephaly Syndrome with Cortical Malformations Associated with Mutations in the WDR62 Gene.
Journal: Genes
Published: February 27, 2021
Genetic testing in Poland and Ukraine: should comprehensive germline testing of BRCA1 and BRCA2 be recommended for women with breast and ovarian cancer?
Journal: Genetics research
Published: August 11, 2020
Phenotypic expansion in Zhu-Tokita-Takenouchi-Kim syndrome caused by de novo variants in the SON gene.
Journal: Molecular genetics & genomic medicine
Published: April 28, 2020
Multiplex ligation-dependent probe amplification as a screening test in children with autism spectrum disorders.
Journal: Advances in clinical and experimental medicine : official organ Wroclaw Medical University
Published: January 29, 2020
Assessment of the FTO gene polymorphisms in male patients with metabolic syndrome.
Journal: Advances in clinical and experimental medicine : official organ Wroclaw Medical University
Published: August 10, 2018
Targeted massively parallel sequencing characterises the mutation spectrum of PALB2 in breast and ovarian cancer cases from Poland and Ukraine.
Journal: Familial cancer
Published: October 21, 2017
Evaluation of a clinical pharmacogenetics model to predict methotrexate response in patients with rheumatoid arthritis.
Journal: The pharmacogenomics journal
Published: August 03, 2017
Last Updated: 09/26/2026