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Ágnes Till

Showing results (1-10 of 17) with videos related to

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Orvosi Hetilap|December 18, 2022
[Neurofibromatosis-1 microdeletion syndrome.]Gergely Büki, Ágnes Till, Anna Zsigmond, et al.
International Journal of Molecular Sciences|September 27, 2025
Uncovering Rare Structural Chromosomal Rearrangements: Insights from Molecular CytogeneticsMárta Czakó, András Szabó, Ágnes Till, et al.
International Journal of Molecular Sciences|June 19, 2024
Case Report of Suspected Gonadal Mosaicism in <i>FOXP1</i>-Related Neurodevelopmental DisorderAnna Zsigmond, Ágnes Till, Judit Bene, et al.
Orvosi Hetilap|December 17, 2019
[<i>MECP2</i> mutation in a male patient identified in the background of severe epileptic encephalopathy]Adrienn Düh, Ágnes Till, Zsolt Bánfai, et al.
International Journal of Molecular Sciences|October 9, 2019
Possible Phenotypic Consequences of Structural Differences in Idic(15) in a Small Cohort of PatientsMárta Czakó, Ágnes Till, András Szabó, et al.
Orvosi Hetilap|December 28, 2020
Gene testing in Treacher Collins syndromeAnna Zsigmond, Ágnes Till, Adrienn Lilla Pintér, et al.
Orvosi Hetilap|November 3, 2015
[Catch-22? Wide variety of phenotypes associated with the chromosome 22q11 deletion syndrome in two patients]Ágnes Till, Kinga Hadzsiev, Anett Lőcsei-Fekete, et al.
Orvosi Hetilap|May 21, 2019
[A rare form of ion channel gene mutation identified as underlying cause of generalized epilepsy]Ágnes Till, Renáta Szalai, Márta Hegyi, et al.
Orvosi Hetilap|March 23, 2017
[A8344G mitochondrial DNA mutation observed in two generations]Anett Fekete, Kinga Hadzsiev, Judit Bene, et al.
International Journal of Molecular Sciences|November 9, 2024
Molecular and Clinical Heterogeneity in Hungarian Patients with Treacher Collins Syndrome-Identification of Two Novel Mutations by Next-Generation SequencingGréta Antal, Anna Zsigmond, Ágnes Till, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Orvosi Hetilap|December 18, 2022
[Neurofibromatosis-1 microdeletion syndrome.]Gergely Büki, Ágnes Till, Anna Zsigmond, et al.
International Journal of Molecular Sciences|September 27, 2025
Uncovering Rare Structural Chromosomal Rearrangements: Insights from Molecular CytogeneticsMárta Czakó, András Szabó, Ágnes Till, et al.
International Journal of Molecular Sciences|June 19, 2024
Case Report of Suspected Gonadal Mosaicism in <i>FOXP1</i>-Related Neurodevelopmental DisorderAnna Zsigmond, Ágnes Till, Judit Bene, et al.
Orvosi Hetilap|December 17, 2019
[<i>MECP2</i> mutation in a male patient identified in the background of severe epileptic encephalopathy]Adrienn Düh, Ágnes Till, Zsolt Bánfai, et al.
International Journal of Molecular Sciences|October 9, 2019
Possible Phenotypic Consequences of Structural Differences in Idic(15) in a Small Cohort of PatientsMárta Czakó, Ágnes Till, András Szabó, et al.
Orvosi Hetilap|December 28, 2020
Gene testing in Treacher Collins syndromeAnna Zsigmond, Ágnes Till, Adrienn Lilla Pintér, et al.
Orvosi Hetilap|November 3, 2015
[Catch-22? Wide variety of phenotypes associated with the chromosome 22q11 deletion syndrome in two patients]Ágnes Till, Kinga Hadzsiev, Anett Lőcsei-Fekete, et al.
Orvosi Hetilap|May 21, 2019
[A rare form of ion channel gene mutation identified as underlying cause of generalized epilepsy]Ágnes Till, Renáta Szalai, Márta Hegyi, et al.
Orvosi Hetilap|March 23, 2017
[A8344G mitochondrial DNA mutation observed in two generations]Anett Fekete, Kinga Hadzsiev, Judit Bene, et al.
International Journal of Molecular Sciences|November 9, 2024
Molecular and Clinical Heterogeneity in Hungarian Patients with Treacher Collins Syndrome-Identification of Two Novel Mutations by Next-Generation SequencingGréta Antal, Anna Zsigmond, Ágnes Till, et al.
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