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Zsolt Tidrenczel

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Fetal and Pediatric Pathology|May 9, 2018
Efficacy of Prenatal Ultrasound in Craniospinal Malformations According to Fetopathological and Postnatal Neonatological, Pathological ResultsFanni Rebeka Eros, Atene Simonyi, Zsolt Tidrenczel, et al.
American Journal of Medical Genetics. Part A|March 8, 2021
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 periodZsolt Tidrenczel, Julia Hajdu, Aténé Simonyi, et al.
Orvosi Hetilap|May 22, 2018
[Prenatally diagnosed case of Pallister‒Killian syndrome]Zsolt Tidrenczel, Erika P Tardy, Edina Sarkadi, et al.
Orvosi Hetilap|March 20, 2022
Genotype-phenotype correlation in a newborn with de novo 3p25 deletion syndromeEdina Sarkadi, Erika P Tardy, Henriett Pikó, et al.
Orvosi Hetilap|July 16, 2023
[Prenatally detected aortic arch anomalies and their consequences after birth]Zsolt Tidrenczel, Erika P Tardy, Anikó Ladányi, et al.
Orvosi Hetilap|March 26, 2019
[Chromosomal microarray comparative genome hybridization (arrayCGH) in prenatal settings. Proposal for Hungarian application in clinical practice]Zsolt Tidrenczel, Erika P Tardy, Henriett Pikó, et al.
Cytogenetic and Genome Research|July 2, 2019
Prenatal Diagnosis of 4q Terminal Deletion and Review of the LiteratureZsolt Tidrenczel, Erika P Tardy, Henriett Pikó, et al.
Orvosi Hetilap|July 18, 2021
The significance of rare chromosomal abnormalities and fetoplacental mosaicism in prenatal diagnosis in the non-invasive prenatal testing eraZsolt Tidrenczel, Erika P Tardy, Ildikó Böjtös, et al.
American Journal of Obstetrics and Gynecology|November 26, 2025
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-analysisMárton Kónya, Ágnes Czimbalmos, Máté Éliás, et al.
Orvosi Hetilap|April 7, 2024
[Summary of the first Hungarian experiences with prenatal chromosomal microarray analysis and whole-exome sequencing]Henriett Pikó, Anett Illés, Sándor Nagy, et al.
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Showing results (1-10 of 10) with videos related to

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Pageof 1
Fetal and Pediatric Pathology|May 9, 2018
Efficacy of Prenatal Ultrasound in Craniospinal Malformations According to Fetopathological and Postnatal Neonatological, Pathological ResultsFanni Rebeka Eros, Atene Simonyi, Zsolt Tidrenczel, et al.
American Journal of Medical Genetics. Part A|March 8, 2021
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 periodZsolt Tidrenczel, Julia Hajdu, Aténé Simonyi, et al.
Orvosi Hetilap|May 22, 2018
[Prenatally diagnosed case of Pallister‒Killian syndrome]Zsolt Tidrenczel, Erika P Tardy, Edina Sarkadi, et al.
Orvosi Hetilap|March 20, 2022
Genotype-phenotype correlation in a newborn with de novo 3p25 deletion syndromeEdina Sarkadi, Erika P Tardy, Henriett Pikó, et al.
Orvosi Hetilap|July 16, 2023
[Prenatally detected aortic arch anomalies and their consequences after birth]Zsolt Tidrenczel, Erika P Tardy, Anikó Ladányi, et al.
Orvosi Hetilap|March 26, 2019
[Chromosomal microarray comparative genome hybridization (arrayCGH) in prenatal settings. Proposal for Hungarian application in clinical practice]Zsolt Tidrenczel, Erika P Tardy, Henriett Pikó, et al.
Cytogenetic and Genome Research|July 2, 2019
Prenatal Diagnosis of 4q Terminal Deletion and Review of the LiteratureZsolt Tidrenczel, Erika P Tardy, Henriett Pikó, et al.
Orvosi Hetilap|July 18, 2021
The significance of rare chromosomal abnormalities and fetoplacental mosaicism in prenatal diagnosis in the non-invasive prenatal testing eraZsolt Tidrenczel, Erika P Tardy, Ildikó Böjtös, et al.
American Journal of Obstetrics and Gynecology|November 26, 2025
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-analysisMárton Kónya, Ágnes Czimbalmos, Máté Éliás, et al.
Orvosi Hetilap|April 7, 2024
[Summary of the first Hungarian experiences with prenatal chromosomal microarray analysis and whole-exome sequencing]Henriett Pikó, Anett Illés, Sándor Nagy, et al.
Pageof 1