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Kinga Hadzsiev

Showing results (11-20 of 91) with videos related to

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Orvosi Hetilap|March 3, 2011
[Molecular genetic diagnosis of neurofibromatosis type I]Noémi Polgár, Katalin Komlósi, Kinga Hadzsiev, et al.
Clinical Dysmorphology|February 22, 2019
Rubinstein-Taybi syndrome 2 with cerebellar abnormality and neural tube defectKinga Hadzsiev, Zsuzsanna Gyorsok, Agnes Till, et al.
Orvosi Hetilap|December 18, 2022
[Neurofibromatosis-1 microdeletion syndrome.]Gergely Büki, Ágnes Till, Anna Zsigmond, et al.
Clinical Dysmorphology|December 1, 2005
Transient progeroid phenotype and lipodystrophy in mosaic polyploidyJudit Kárteszi, György Kosztolányi, Marta Czakó, 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.
BMC Genetics|September 2, 2017
Refining the South Asian Origin of the Romani peopleBela I Melegh, Zsolt Banfai, Kinga Hadzsiev, et al.
Archives of Dermatology|May 18, 2005
A patient with Rothmund-Thomson syndrome and all features of RAPADILINORichard Kellermayer, H Annika Siitonen, Kinga Hadzsiev, 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|March 21, 2008
[Psychological aspects of presymptomatic diagnosis in Huntington disease]Berta Bondor, Judit Kárteszi, Kinga Hadzsiev, et al.
Molecular Cytogenetics|June 26, 2015
Partial tetrasomy of the proximal long arm of chromosome 15 in two patients: the significance of the gene dosage in terms of phenotypeAndras Szabo, Marta Czako, Kinga Hadzsiev, et al.
Pageof 10

Showing results (11-20 of 91) with videos related to

Sort By:
Pageof 10
Orvosi Hetilap|March 3, 2011
[Molecular genetic diagnosis of neurofibromatosis type I]Noémi Polgár, Katalin Komlósi, Kinga Hadzsiev, et al.
Clinical Dysmorphology|February 22, 2019
Rubinstein-Taybi syndrome 2 with cerebellar abnormality and neural tube defectKinga Hadzsiev, Zsuzsanna Gyorsok, Agnes Till, et al.
Orvosi Hetilap|December 18, 2022
[Neurofibromatosis-1 microdeletion syndrome.]Gergely Büki, Ágnes Till, Anna Zsigmond, et al.
Clinical Dysmorphology|December 1, 2005
Transient progeroid phenotype and lipodystrophy in mosaic polyploidyJudit Kárteszi, György Kosztolányi, Marta Czakó, 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.
BMC Genetics|September 2, 2017
Refining the South Asian Origin of the Romani peopleBela I Melegh, Zsolt Banfai, Kinga Hadzsiev, et al.
Archives of Dermatology|May 18, 2005
A patient with Rothmund-Thomson syndrome and all features of RAPADILINORichard Kellermayer, H Annika Siitonen, Kinga Hadzsiev, 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|March 21, 2008
[Psychological aspects of presymptomatic diagnosis in Huntington disease]Berta Bondor, Judit Kárteszi, Kinga Hadzsiev, et al.
Molecular Cytogenetics|June 26, 2015
Partial tetrasomy of the proximal long arm of chromosome 15 in two patients: the significance of the gene dosage in terms of phenotypeAndras Szabo, Marta Czako, Kinga Hadzsiev, et al.
Pageof 10