Zsolt Tidrenczel
Magyar Honvédség Egészségügyi Központ Budapest, Puerto Rico
Last Updated: 09/26/2026
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Found 10 publications
Discordant findings in genome-wide non-invasive prenatal testing (GW-NIPT) for rare chromosomal abnormalities, adverse pregnancy outcomes, and maternal malignancies: a systematic review and meta-analysis.
Journal: American journal of obstetrics and gynecology
Published: July 10, 2025
Prenatally detected aortic arch anomalies and their consequences after birth
Journal: Orvosi hetilap
Published: March 03, 2023
Genotype-phenotype correlation in a newborn with de novo 3p25 deletion syndrome
Journal: Orvosi hetilap
Published: August 19, 2021
The significance of rare chromosomal abnormalities and fetoplacental mosaicism in prenatal diagnosis in the non-invasive prenatal testing era
Journal: Orvosi hetilap
Published: October 28, 2020
Trends in the prenatal diagnosis of trisomy 21 show younger maternal age and shift in the distribution of congenital heart disease over a 20-year period.
Journal: American journal of medical genetics. Part A
Published: March 03, 2020
Chromosomal microarray comparative genome hybridization (arrayCGH) in prenatal settings. Proposal for Hungarian application in clinical practice
Journal: Orvosi hetilap
Published: March 26, 2019
Prenatal Diagnosis of 4q Terminal Deletion and Review of the Literature.
Journal: Cytogenetic and genome research
Published: February 12, 2019
Prenatally diagnosed case of Pallister‒Killian syndrome
Journal: Orvosi hetilap
Published: May 22, 2018
Efficacy of Prenatal Ultrasound in Craniospinal Malformations According to Fetopathological and Postnatal Neonatological, Pathological Results.
Journal: Fetal and pediatric pathology
Published: May 09, 2018
Showing 1-10 of 10
Last Updated: 09/26/2026