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Pikó, Henriett
37
results:
Search for persons
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Online (37)
Mediatypes
Articles (Online) (22)
OpenAccess-fulltext (15)
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english (29)
Sorted by: Relevance
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1
Screening of premature ovarian insufficiency associated gen..:
Illés, Anett
;
Pikó, Henriett
;
Árvai, Kristóf
...
BMC Medical Genomics. 17 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1186/..
?
2
Genetic Factors Associated with the Development of Neuropat..:
Tordai, Dóra Zsuszanna
;
Hajdú, Noémi
;
Rácz, Ramóna
...
International Journal of Molecular Sciences. 25 (2024) 3 - p. 1815 , 2024
Link:
https://doi.org/10.3390/..
?
3
Az első hazai tapasztalatok összegzése kromoszomális microa..:
Pikó, Henriett
;
Illés, Anett
;
Nagy, Sándor
...
Orvosi Hetilap. 165 (2024) 14 - p. 523-530 , 2024
Link:
https://doi.org/10.1556/..
?
4
Heterogenic Genetic Background of Distal Arthrogryposis—Rev..:
Illés, Anett
;
Pikó, Henriett
;
Bartek, Virág
...
Children. 11 (2024) 7 - p. 861 , 2024
Link:
https://doi.org/10.3390/..
?
5
Analysis of SIRT1 Gene SNPs and Clinical Characteristics in..:
Bojtor, Bence
;
Vaszilko, Mihaly
;
Armos, Richard
...
International Journal of Molecular Sciences. 25 (2024) 7 - p. 3646 , 2024
Link:
https://doi.org/10.3390/..
?
6
Misfolding of fukutin-related protein (FKRP) variants in co..:
Esapa, Christopher T.
;
McIlhinney, R. A. Jeffrey
;
Waite, Adrian J.
...
Frontiers in Molecular Biosciences. 10 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
7
Comparison of surgical strategies in the treatment of low-r..:
Kiss, András
;
Szili, Balázs
;
Bakos, Bence
...
BMC Endocrine Disorders. 23 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1186/..
?
8
De novo 3p25-deletiós szindróma genotípus-fenotípus vizsgál..:
Sarkadi, Edina
;
P. Tardy, Erika
;
Pikó, Henriett
...
Orvosi Hetilap. 163 (2022) 12 - p. 478-483 , 2022
Link:
https://doi.org/10.1556/..
?
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
A ritka kromoszóma-rendellenességek és a fetoplacentaris mo..:
Tidrenczel, Zsolt
;
P. Tardy, Erika
;
Böjtös, Ildikó
...
Orvosi Hetilap. 162 (2021) 29 - p. 1156-1165 , 2021
Link:
https://doi.org/10.1556/..
?
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
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/..
?
13
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/..
?
14
Validation of the United Kingdom copy-number alteration cla..:
Hamadeh, Lina
;
Enshaei, Amir
;
Schwab, Claire
...
Blood Advances. 3 (2019) 2 - p. 148-157 , 2019
Link:
https://doi.org/10.1182/..
?
15
Study of patterns of inheritance of premature ovarian failu..:
Beke, Artur
;
Piko, Henriett
;
Haltrich, Iren
...
BMC Medical Genetics. 19 (2018) 1 - p. , 2018
Link:
https://doi.org/10.1186/..
1-15