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Kinga Hadzsiev

Showing results (1-10 of 91) with videos related to

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Current Medicinal Chemistry|August 13, 2016
Cytochrome P450 Drug Metabolizing Enzymes in Roma Population Samples: Systematic Review of the LiteratureRenata Szalai, Kinga Hadzsiev, Bela Melegh
Current Molecular Medicine|April 11, 2023
Microhomology-Mediated Break-Induced Replication: A Possible Molecular Mechanism of the Formation of a Large CNV in <i>FBN1</i> Gene in a Patient with Marfan SyndromeGergely Buki, Kinga Hadzsiev, Judit Bene
Nutrition & Diabetes|March 18, 2018
Role of carnitine and its derivatives in the development and management of type 2 diabetesJudit Bene, Kinga Hadzsiev, Bela Melegh
International Journal of Molecular Sciences|September 28, 2023
Copy Number Variations in Neuropsychiatric DisordersGergely Büki, Kinga Hadzsiev, Judit Bene
Magyar Onkologia|March 18, 2020
[When is it necessary to refer a child with cancer to genetic counseling?]Réka Ripszám, Béla Melegh, Kinga Hadzsiev
Gene|May 2, 2012
Jumping translocation of 15q24-qter resulting in partial trisomy: a case reportMárta Czakó, Kinga Hadzsiev, Béla Melegh, et al.
Orvosi Hetilap|January 22, 2013
[Larsen-syndrome: final diagnosis following multiple surgical interventions]Péter Kisfali, Katalin Komlósi, Kinga Hadzsiev, et al.
Acta Biologica Hungarica|May 2, 2006
Excess of malignancies in grandparents of children with malformations? Short communicationKinga Hadzsiev, A Tárnok, G Kosztolányi, et al.
Orvosi Hetilap|July 17, 2007
[Rapid diagnosis of fetal chromosomal abnormalities by fluorescence in situ hybridization]Kinga Hadzsiev, Márta Czakó, Béla Veszprémi, et al.
Molecular Genetics and Metabolism Reports|March 12, 2024
Importance and application of WES in fetal genetic diagnostics: Identification of novel <i>ASPM</i> mutation in a fetus with microcephalyRenata Szalai, Agnes Till, Attila Gyenesei, et al.
Pageof 10

Showing results (1-10 of 91) with videos related to

Sort By:
Pageof 10
Current Medicinal Chemistry|August 13, 2016
Cytochrome P450 Drug Metabolizing Enzymes in Roma Population Samples: Systematic Review of the LiteratureRenata Szalai, Kinga Hadzsiev, Bela Melegh
Current Molecular Medicine|April 11, 2023
Microhomology-Mediated Break-Induced Replication: A Possible Molecular Mechanism of the Formation of a Large CNV in <i>FBN1</i> Gene in a Patient with Marfan SyndromeGergely Buki, Kinga Hadzsiev, Judit Bene
Nutrition & Diabetes|March 18, 2018
Role of carnitine and its derivatives in the development and management of type 2 diabetesJudit Bene, Kinga Hadzsiev, Bela Melegh
International Journal of Molecular Sciences|September 28, 2023
Copy Number Variations in Neuropsychiatric DisordersGergely Büki, Kinga Hadzsiev, Judit Bene
Magyar Onkologia|March 18, 2020
[When is it necessary to refer a child with cancer to genetic counseling?]Réka Ripszám, Béla Melegh, Kinga Hadzsiev
Gene|May 2, 2012
Jumping translocation of 15q24-qter resulting in partial trisomy: a case reportMárta Czakó, Kinga Hadzsiev, Béla Melegh, et al.
Orvosi Hetilap|January 22, 2013
[Larsen-syndrome: final diagnosis following multiple surgical interventions]Péter Kisfali, Katalin Komlósi, Kinga Hadzsiev, et al.
Acta Biologica Hungarica|May 2, 2006
Excess of malignancies in grandparents of children with malformations? Short communicationKinga Hadzsiev, A Tárnok, G Kosztolányi, et al.
Orvosi Hetilap|July 17, 2007
[Rapid diagnosis of fetal chromosomal abnormalities by fluorescence in situ hybridization]Kinga Hadzsiev, Márta Czakó, Béla Veszprémi, et al.
Molecular Genetics and Metabolism Reports|March 12, 2024
Importance and application of WES in fetal genetic diagnostics: Identification of novel <i>ASPM</i> mutation in a fetus with microcephalyRenata Szalai, Agnes Till, Attila Gyenesei, et al.
Pageof 10