E-LIB Suche - Ergebnisse für: Pikó, Henriett

1

Az első hazai tapasztalatok összegzése kromoszomális microa..:

Pikó, Henriett ; Illés, Anett ; Nagy, Sándor...
Orvosi Hetilap. 165 (2024) 14 - p. 523-530 , 2024

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

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/..

4

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/..

5

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/..

6

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/..

7

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/..

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

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/..

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

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/..

12

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/..

13

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/..

14

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/..

15

Complex X chromosome rearrangement associated with multiorg..:

Haltrich, Irén ; Pikó, Henriett ; Pamjav, Horolma...
Molecular Cytogenetics. 8 (2015) 1 - p. , 2015

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