Magdalena Pasinska
Torun, KP, Poland
Last Updated: 09/26/2026
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Found 16 publications
Germline predisposition to acute myeloid leukemia in polish patients.
Journal: Leukemia & lymphoma
Published: October 27, 2025
Distinguishing benign from pathogenic duplications involving GPR101 and VGLL1-adjacent enhancers in the clinical setting with the bioinformatic tool POSTRE.
Journal: NPJ genomic medicine
Published: July 10, 2025
Distinguishing benign from pathogenic duplications involving GPR101 and VGLL1-adjacent enhancers in the clinical setting with the bioinformatic tool POSTRE.
Journal: medRxiv : the preprint server for health sciences
Published: July 09, 2025
Case Report: Hypergonadotropic hypogonadism in an elite athlete with variant in FSH receptor gene-clinical and sports implications of proper diagnosis.
Journal: Frontiers in endocrinology
Published: June 17, 2025
Familial 3M Syndrome - as an Example of Diagnostic Difficulties in Rare Genetic Syndromes.
Journal: The application of clinical genetics
Published: May 31, 2025
Novel compound heterozygous FAM20C variants cause Raine syndrome - retrospective prenatal diagnosis and literature review.
Journal: Orphanet journal of rare diseases
Published: April 14, 2025
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
Clinical Importance of aCGH in Genetic Counselling of Children with Psychomotor Retardation.
Journal: The application of clinical genetics
Published: January 22, 2022
Abnormal sperm morphology is associated with sensitization to inhaled allergens.
Journal: International journal of immunopathology and pharmacology
Published: January 05, 2022
Prenatal identification of partial 3q duplication syndrome.
Journal: BMC medical genomics
Published: August 15, 2018
Multiple occurrence of psychomotor retardation and recurrent miscarriages in a family with a submicroscopic reciprocal translocation t(7;17)(p22;p13.2).
Journal: BMC medical genomics
Published: July 26, 2018
Complex balanced chromosomal translocation t(2;5;13) (p21;p15;q22) in a woman with four reproductive failures.
Journal: Molecular cytogenetics
Published: August 19, 2014
Last Updated: 09/26/2026