Anna Repczynska
Torun, KP, Poland
Last Updated: 09/26/2026
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Found 8 publications
Novel compound heterozygous FAM20C variants cause Raine syndrome - retrospective prenatal diagnosis and literature review.
Journal: Orphanet journal of rare diseases
Published: April 14, 2025
New Insights into the Fanconi Anemia Pathogenesis: A Crosstalk Between Inflammation and Oxidative Stress.
Journal: International journal of molecular sciences
Published: September 30, 2024
Cytogenetic findings in Polish patients with suspected Fanconi anemia.
Journal: Advances in clinical and experimental medicine : official organ Wroclaw Medical University
Published: February 12, 2023
The Levels of Pregnancy-Associated Plasma Protein (PAPP-A) and Chorionic Gonadotropin (β-hCG) in the Blood Serum of Women with Hypothyroidism in the 1st Trimester of Pregnancy.
Journal: International journal of women's health
Published: September 12, 2022
Next-generation sequencing reveals novel variants and large deletion in FANCA gene in Polish family with Fanconi anemia.
Journal: Orphanet journal of rare diseases
Published: March 03, 2022
Clinical Importance of aCGH in Genetic Counselling of Children with Psychomotor Retardation.
Journal: The application of clinical genetics
Published: January 22, 2022
Prenatal identification of partial 3q duplication syndrome.
Journal: BMC medical genomics
Published: August 15, 2018
Showing 1-8 of 8
Last Updated: 09/26/2026