All Stories

  1. First Hungarian experiences with prenatal chromosomal microarray analysis and whole-exome sequencing

    Article • Orvosi Hetilap, April 2024, Akademiai Kiado

    Dr Zsolt Tidrenczel

  2. Prenatally detected aortic arch anomalies and their consequences after birth

    Article • Orvosi Hetilap, July 2023, Akademiai Kiado

    Dr Zsolt Tidrenczel

  3. Genotype-phenotype correlation in a newborn with de novo 3p25 deletion syndrome

    Article • Orvosi Hetilap, March 2022, Akademiai Kiado

    Dr Zsolt Tidrenczel

  4. The significance of rare chromosomal abnormalities and fetoplacental mosaicism in prenatal diagnosis

    Article • Orvosi Hetilap, July 2021, Akademiai Kiado

    Dr Zsolt Tidrenczel

  5. 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

    Article • American Journal of Medical Genetics Part A, March 2021, Wiley

    Dr Zsolt Tidrenczel

  6. Hungarian application of prenatal Chromosomal microarray comparative genome hybridization (arrayCGH)

    Article • Orvosi Hetilap, March 2019, Akademiai Kiado

    Dr Zsolt Tidrenczel

  7. Prenatal Diagnosis of 4q Terminal Deletion

    Article • Cytogenetic and Genome Research, January 2019, Karger Publishers

    Dr Zsolt Tidrenczel

  8. Efficacy of Prenatal Ultrasound in Craniospinal Malformations According to Fetopathological and Postnatal Neonatological, Pathological Results

    Article • Fetal and Pediatric Pathology, May 2018, Taylor & Francis

    Dr Zsolt Tidrenczel

  9. Prenatally diagnosed case of Pallister‒Killian syndrome

    Article • Orvosi Hetilap, May 2018, Akademiai Kiado

    Dr Zsolt Tidrenczel