Pawel Borun
Poznan, WP, Poland
Last Updated: 09/26/2026
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Found 11 publications
Modifying impact of RET gene haplotypes on medullary thyroid carcinoma clinical course.
Journal: Endocrine-related cancer
Published: January 23, 2018
New EPCAM founder deletion in Polish population.
Journal: Clinical genetics
Published: December 18, 2016
A Simple Method for TPMT and ITPA Genotyping Using Multiplex HRMA for Patients Treated with Thiopurine Drugs.
Journal: Molecular diagnosis & therapy
Published: June 17, 2016
Rapid Detection Method for the Four Most Common CHEK2 Mutations Based on Melting Profile Analysis.
Journal: Molecular diagnosis & therapy
Published: October 09, 2015
Specific Alu elements involved in a significant percentage of copy number variations of the STK11 gene in patients with Peutz-Jeghers syndrome.
Journal: Familial cancer
Published: April 06, 2015
Hamartomatous polyposis syndromes.
Journal: Hereditary cancer in clinical practice
Published: March 14, 2013
Familial adenomatous polyposis of the colon.
Journal: Hereditary cancer in clinical practice
Published: March 14, 2013
High-resolution melting analysis of the TPMT gene: a study in the Polish population.
Journal: Genetic testing and molecular biomarkers
Published: December 21, 2012
High Resolution Melting analysis as a rapid and efficient method of screening for small mutations in the STK11 gene in patients with Peutz-Jeghers syndrome.
Journal: BMC medical genetics
Published: November 23, 2012
Absence of the RET+3:T allele in the MTC patients.
Journal: Hereditary cancer in clinical practice
Published: May 29, 2012
Showing 1-11 of 11
Last Updated: 09/26/2026