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Haltrich, Irén
65
results:
Search for persons
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Format
Online (65)
Mediatypes
Articles (Online) (25)
Bookchapter (Online) (3)
OpenAccess-fulltext (37)
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english (60)
Sorted by: Relevance
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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/..
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2
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/..
?
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
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/..
?
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
Contributors:
, In:
Twin Research for Everyone
,
Almqvist, Catarina
;
Ando, Juko
;
Bartels, Meike
... - p. xxiii-xxx , 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
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/..
?
9
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/..
?
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
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/..
?
12
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/..
?
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/..
1-15