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Magyar Onkologia|December 10, 2024
[The role of cytogenetic tests in the diagnosis of malignant hematologic diseases]Anikó UjfalusiEJIFCC|July 3, 2019
The role of microRNAs in congenital heart diseaseOrsolya Nagy, Sándor Baráth, Anikó UjfalusiJournal of Human Reproductive Sciences|February 22, 2019
Examination of Y-Chromosomal Microdeletions and Partial Microdeletions in Idiopathic Infertility in East Hungarian PatientsAttila Mokánszki, Anikó Ujfalusi, Éva Gombos, et al.Frontiers in Pediatrics|September 7, 2021
Case Report: Expressive Speech Disorder in a Family as a Hallmark of 7q31 Deletion Involving the <i>FOXP2</i> GeneOrsolya Nagy, Judit Kárteszi, Beatrix Elmont, et al.Genes|November 11, 2022
Cytogenetic Investigation of Infertile Patients in Hungary: A 10-Year Retrospective StudySzilvia Andó, Katalin Koczok, Beáta Bessenyei, et al.Cold Spring Harbor Molecular Case Studies|October 16, 2021
<i>MED13L</i>-related intellectual disability due to paternal germinal mosaicismBeáta Bessenyei, István Balogh, Attila Mokánszki, et al.Orvosi Hetilap|June 19, 2010
[Detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation]Gabriella P Szabó, Beáta Bessenyei, Erzsébet Balogh, et al.American Journal of Medical Genetics. Part A|March 13, 2012
Subtelomeric 6.7 Mb trisomy 10p and 5.6 Mb monosomy 21q detected by FISH and array-CGH in three related patientsGabriella P Szabó, Alida C Knegt, Anikó Ujfalusi, et al.Applied Immunohistochemistry & Molecular Morphology : AIMM|May 19, 2012
Identification of NPMc+ acute myeloid leukemia in bone marrow smearsJudit Bedekovics, László Rejtő, Béla Telek, et al.Diagnostic Pathology|July 26, 2024
Extracranial metastatic oligodendroglioma with molecular progression, case presentationNour Kurdi, Attila Mokánszki, Ingrid Balogh, et al.Pageof 5