Magdalena Glaska-Bartnik
17a Kasprzaka Street
Warsaw, MZ 01211, Poland
Warsaw, MZ 01211, Poland
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 11 publications
Cytogenomic features of Richter transformation.
Journal: Molecular cytogenetics
Published: August 02, 2023
Coexisting Conditions Modifying Phenotypes of Patients with 22q11.2 Deletion Syndrome.
Journal: Genes
Published: November 19, 2022
Comparative Genomic Hybridization to Microarrays in Fetuses with High-Risk Prenatal Indications: Polish Experience with 7400 Pregnancies.
Journal: Genes
Published: March 19, 2022
Application of array comparative genomic hybridization (aCGH) for identification of chromosomal aberrations in the recurrent pregnancy loss.
Journal: Journal of assisted reproduction and genetics
Published: November 03, 2021
How does terminal 21q22 deletion really manifest? Delineation based on prenatal diagnosis and literature review.
Journal: Taiwanese journal of obstetrics & gynecology
Published: June 13, 2021
The MED13L haploinsufficiency syndrome associated with de novo nonsense variant (P.GLN1981*).
Journal: Journal of mother and child
Published: April 30, 2021
A placental trisomy 2 detected by NIPT evolved in a fetal small Supernumerary Marker Chromosome (sSMC).
Journal: Molecular cytogenetics
Published: December 04, 2020
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
Diagnostic implications of genetic copy number variation in epilepsy plus.
Journal: Epilepsia
Published: May 18, 2018
Phenotypic consequences of gene disruption by a balanced de novo translocation involving SLC6A1 and NAA15.
Journal: European journal of medical genetics
Published: February 05, 2018
Showing 1-11 of 11
Last Updated: 09/26/2026