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Erika P Tardy

Showing results (1-10 of 7) with videos related to

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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.
Orvosi Hetilap|August 10, 2007
[Mixed gonadal dysgenesis associated with an isodicentric Y chromosome]László Ságodi, Enikô Sólyom, András Tóth, 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.
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.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
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.
Orvosi Hetilap|August 10, 2007
[Mixed gonadal dysgenesis associated with an isodicentric Y chromosome]László Ságodi, Enikô Sólyom, András Tóth, 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.
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.
Pageof 1