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Pinti, Éva
30
results:
Search for persons
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Format
Online (30)
Mediatypes
Articles (Online) (10)
OpenAccess-fulltext (20)
Languages
english (26)
Sorted by: Relevance
Sorted by: Year
?
1
A Cross-Sectional Study of the Dermatological Manifestation..:
Anker, Pálma
;
Fésűs, Luca
;
Kiss, Norbert
...
Diagnostics. 13 (2023) 14 - p. 2368 , 2023
Link:
https://doi.org/10.3390/..
?
2
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/..
?
3
Microdeletions in 1q21 and 8q12.1 depict two additional mol..:
Baba, Naomi
;
Lengyel, Anna
;
Pinti, Eva
...
Molecular Cytogenetics. 15 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1186/..
?
4
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/..
?
5
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/..
?
6
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/..
?
7
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/..
?
8
Frequency of KCNQ1 variants causing loss of methylation of ..:
Eßinger, Carla
;
Karch, Stephanie
;
Moog, Ute
...
Clinical Epigenetics. 12 (2020) 1 - p. , 2020
Link:
https://doi.org/10.1186/..
?
9
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/..
?
10
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/..
?
11
An Ultra-Rare Manifestation of an X-Linked Recessive Disord..:
Szűcs, Zsuzsanna
;
Pinti, Éva
;
Haltrich, Irén
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9655586/. , 2022
Link:
http://www.ncbi.nlm.nih...
?
12
Microdeletions in 1q21 and 8q12.1 depict two additional mol..:
Baba, Naomi
;
Lengyel, Anna
;
Pinti, Eva
...
info:eu-repo/semantics/altIdentifier/pmid/pmid:35562807. , 2022
Link:
https://publications.rwt..
?
13
An Ultra-Rare Manifestation of an X-Linked Recessive Disord..:
Szűcs, Zsuzsanna
;
Pinti, Éva
;
Haltrich, Irén
...
International Journal Of Molecular Sciences. -23 : 21 (2022), p. 1-15. -Int. J. Mol. Sci. - 1422-0067. , 2022
Link:
https://hdl.handle.net/2..
?
14
Microdeletions in 1q21 and 8q12.1 depict two additional mol..:
Baba, Naomi
;
Lengyel, Anna
;
Pinti, Eva
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9107271/. , 2022
Link:
http://www.ncbi.nlm.nih...
?
15
Clinical evaluation of rare copy number variations identifi..:
Lengyel, Anna
;
Pinti, Éva
;
Pikó, Henriett
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9623912/. , 2022
Link:
http://www.ncbi.nlm.nih...
1-15