E-LIB Suche - Ergebnisse für: Haltrich, Irén

1

Hypodiploidy has unfavorable impact on survival in pediatri..:

Hammer, Anne Sofie Borg ; Juul-Dam, Kristian Løvvik ; Sandahl, Julie Damgaard...
Blood Advances. 7 (2023) 6 - p. 1045-1055 , 2023

Link: https://doi.org/10.1182/..

2

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/..

3

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/..

4

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/..

5

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/..

6

Chromosomal anomalies, monogenetic diseases, and leukaemia ..:

, In: Twin Research for Everyone,

Haltrich, Irén ; Lengyel, Anna - p. 665-686 , 2022

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

7

A 22q11.2-microdeletiós szindróma klinikai jellemzői:

Szumutku, Fanni ; Kádár, Krisztina ; Kovács, Árpád Ferenc...
Orvosi Hetilap. 163 (2022) 1 - p. 21-30 , 2022

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

8

Clinical evaluation of rare copy number variations identifi..:

Lengyel, Anna ; Pinti, Éva ; Pikó, Henriett...
Molecular Cytogenetics. 15 (2022) 1 - p. , 2022

Link: https://doi.org/10.1186/..

9

Contributors:

, In: Twin Research for Everyone,

Almqvist, Catarina ; Ando, Juko ; Bartels, Meike... - p. xxiii-xxx , 2022

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

10

Generation of multiple iPSC clones from a male schizophreni..:

Hathy, Edit ; Szabó, Eszter ; Vincze, Katalin...
Stem Cell Research. 51 (2021) - p. 102140 , 2021

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

11

Diagnostic difficulties and possibilities of NF1-like syndr..:

Pinti, Eva ; Nemeth, Krisztina ; Staub, Krisztina...
BMC Pediatrics. 21 (2021) 1 - p. , 2021

Link: https://doi.org/10.1186/..

12

Chromosome 2q14.3 microdeletion encompassing CNTNAP5 gene i..:

Lengyel, Anna ; Pinti, Éva ; Nebral, Karin...
Journal of Genetics. 100 (2021) 2 - p. , 2021

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

13

Clinical and genetic findings in Hungarian pediatric patien..:

Lengyel, Anna ; Pinti, Éva ; Pikó, Henriett...
European Journal of Medical Genetics. 63 (2020) 10 - p. 104027 , 2020

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

14

Comprehensive profiling of disease-relevant copy number abe..:

Kiss, Richárd ; Gángó, Ambrus ; Benard-Slagter, Anne...
Modern Pathology. 33 (2020) 5 - p. 812-824 , 2020

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

15

What should we consider in the case of combined Down- and 4..:

Pinti, Eva ; Lengyel, Anna ; Fekete, Gyorgy.
BMC Pediatrics. 20 (2020) 1 - p. , 2020

Link: https://doi.org/10.1186/..