E-LIB Suche - Ergebnisse für: Ujfalusi, Anikó

1

A JAK2 szomatikus génmutáció lehetséges betegségmódosító ha..:

Magyar, Eszter ; Újfalusi, Anikó ; Czenke, Marianna.
Orvosi Hetilap. 165 (2024) 23 - p. 883-890 , 2024

Link: https://doi.org/10.1556/..

2

Enhancing HLA‐B27 antigen detection: Leveraging machine lea..:

Baráth, Sándor ; Singh, Parvind ; Hevessy, Zsuzsanna...
Cytometry Part B: Clinical Cytometry. , 2024

Link: https://doi.org/10.1002/..

3

PB1699: GENOMIC AND TRANSCRIPTOMIC PROFILING REVEALS NOVEL ..:

Péterffy, Borbála ; Krizsán, Szilvia ; Egyed, Bálint...
HemaSphere. 7 (2023) S3 - p. e5932101 , 2023

Link: https://doi.org/10.1097/..

4

Next-Generation Sequencing–Based Genomic Profiling of Child..:

Krizsán, Szilvia ; Péterffy, Borbála ; Egyed, Bálint...
The Journal of Molecular Diagnostics. 25 (2023) 8 - p. 555-568 , 2023

Link: https://doi.org/10.1016/..

5

PersonALL: a genetic scoring guide for personalized risk as..:

Bedics, Gábor ; Egyed, Bálint ; Kotmayer, Lili...
British Journal of Cancer. 129 (2023) 3 - p. 455-465 , 2023

Link: https://doi.org/10.1038/..

6

Helsmoortel–Van der Aa Syndrome—Cardiothoracic and Ectoderm..:

Szabó, Tímea Margit ; Balogh, István ; Ujfalusi, Anikó...
Genes. 13 (2022) 12 - p. 2367 , 2022

Link: https://doi.org/10.3390/..

7

An Ultra-Rare Manifestation of an X-Linked Recessive Disord..:

Szűcs, Zsuzsanna ; Pinti, Éva ; Haltrich, Irén...
International Journal of Molecular Sciences. 23 (2022) 21 - p. 13076 , 2022

Link: https://doi.org/10.3390/..

8

Cytogenetic Investigation of Infertile Patients in Hungary:..:

Andó, Szilvia ; Koczok, Katalin ; Bessenyei, Beáta..
Genes. 13 (2022) 11 - p. 2086 , 2022

Link: https://doi.org/10.3390/..

9

Deep Molecular and In Silico Protein Analysis of p53 Altera..:

Madarász, Kristóf ; Mótyán, János András ; Bedekovics, Judit...
Cells. 11 (2022) 21 - p. 3475 , 2022

Link: https://doi.org/10.3390/..

10

A Novel Method for the Evaluation of Bone Marrow Samples fr..:

Kárai, Bettina ; Tisza, Katalin ; Eperjesi, Orsolya...
Cancers. 13 (2021) 20 - p. 5044 , 2021

Link: https://doi.org/10.3390/..

11

Greig Cephalopolysyndactyly Contiguous Gene Syndrome: Case ..:

Kozma, Kinga ; Bembea, Marius ; Jurca, Claudia M....
Genes. 12 (2021) 11 - p. 1674 , 2021

Link: https://doi.org/10.3390/..

12

Az IGHV-mutációs státusz vizsgálata a Magyar Hematológiai é..:

Nagy, Ákos ; Andrikovics, Hajnalka ; Kajtár, Béla...
Hematológia–Transzfuziológia. 54 (2021) 2 - p. 75-80 , 2021

Link: https://doi.org/10.1556/..

13

Hereditary and non-hereditary etiologies associated with ex..:

Salamon, András ; Zádori, Dénes ; Ujfalusi, Anikó...
Metabolic Brain Disease. 36 (2021) 7 - p. 2131-2139 , 2021

Link: https://doi.org/10.1007/..

14

Case Report: Expressive Speech Disorder in a Family as a Ha..:

Nagy, Orsolya ; Kárteszi, Judit ; Elmont, Beatrix.
Frontiers in Pediatrics. 9 (2021) - p. , 2021

Link: https://doi.org/10.3389/..

15

Systemic Screening for 22q11.2 Copy Number Variations in Hu..:

Zodanu, Gloria Kafui Esi ; Oszlánczi, Mónika ; Havasi, Kálmán...
Frontiers in Genetics. 12 (2021) - p. , 2021

Link: https://doi.org/10.3389/..