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LAŠTŮVKOVÁ, JANA
28
results:
Search for persons
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Format
Online (28)
Mediatypes
Articles (Online) (13)
OpenAccess-fulltext (15)
Sorted by: Year
Sorted by: Relevance
?
1
A founder COL4A4 pathogenic variant resulting in autosomal ..:
Plevova, Pavlina
;
Indrakova, Jana
;
Savige, Judy
...
Frontiers in Medicine. 10 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
2
A founder COL4A4 pathogenic variant resulting in autosomal ..:
Plevova, Pavlina
;
Indrakova, Jana
;
Savige, Judy
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9948603/. , 2023
Link:
http://www.ncbi.nlm.nih...
?
3
Data_Sheet_2_A founder COL4A4 pathogenic variant resulting ..:
Pavlina Plevova
;
Jana Indrakova
;
Judy Savige
...
doi:10.3389/fmed.2023.1096869.s002. , 2023
Link:
https://doi.org/10.3389/..
?
4
A founder COL4A4 pathogenic variant resulting in autosomal ..:
Pavlina Plevova
;
Jana Indrakova
;
Judy Savige
...
https://www.frontiersin.org/articles/10.3389/fmed.2023.1096869/full. , 2023
Link:
https://doi.org/10.3389/..
?
5
Data_Sheet_1_A founder COL4A4 pathogenic variant resulting ..:
Pavlina Plevova
;
Jana Indrakova
;
Judy Savige
...
doi:10.3389/fmed.2023.1096869.s001. , 2023
Link:
https://doi.org/10.3389/..
?
6
Data_Sheet_1_A founder COL4A4 pathogenic variant resulting ..:
Pavlina Plevova
;
Jana Indrakova
;
Judy Savige
...
doi:10.3389/fmed.2023.1096869.s001. , 2023
Link:
https://doi.org/10.3389/..
?
7
Data_Sheet_2_A founder COL4A4 pathogenic variant resulting ..:
Pavlina Plevova
;
Jana Indrakova
;
Judy Savige
...
doi:10.3389/fmed.2023.1096869.s002. , 2023
Link:
https://doi.org/10.3389/..
?
8
Czech family confirms the new 1p36.13‐1p36.12 microdeletion..:
Seeman, Pavel
;
Čejnová, Vlasta
;
Černá, Šárka
...
Clinical Genetics. 102 (2022) 3 - p. 244-245 , 2022
Link:
https://doi.org/10.1111/..
?
9
The Cause of Hereditary Hearing Loss in GJB2 Heterozygotes—..:
Safka Brozkova, Dana
;
Uhrova Meszarosova, Anna
;
Lassuthova, Petra
...
Genes. 12 (2021) 5 - p. 684 , 2021
Link:
https://doi.org/10.3390/..
?
10
The Cause of Hereditary Hearing Loss in GJB2 Heterozygotes—..:
Dana Safka Brozkova
;
Anna Uhrova Meszarosova
;
Petra Lassuthova
...
Human Genomics and Genetic Diseases. , 2021
Link:
https://doi.org/10.3390/..
?
11
The Cause of Hereditary Hearing Loss in GJB2 Heterozygotes—..:
Dana Safka Brozkova
;
Anna Uhrova Meszarosova
;
Petra Lassuthova
...
https://www.mdpi.com/2073-4425/12/5/684. , 2021
Link:
https://doi.org/10.3390/..
?
12
The Cause of Hereditary Hearing Loss in GJB2 Heterozygotes—..:
Safka Brozkova, Dana
;
Uhrova Meszarosova, Anna
;
Lassuthova, Petra
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8147375/. , 2021
Link:
http://www.ncbi.nlm.nih...
?
13
Fatal neonatal nephrocutaneous syndrome in 18 Roma children..:
Mazurova, Stella
;
Tesarova, Marketa
;
Zeman, Jiri
...
The Journal of Dermatology. 47 (2020) 6 - p. 663-668 , 2020
Link:
https://doi.org/10.1111/..
?
14
Spectrum and frequencies of non GJB2 gene mutations in Czec..:
Safka Brozkova, Dana
;
Poisson Marková, Simona
;
Mészárosová, Anna Uhrová
...
Clinical Genetics. 98 (2020) 6 - p. 548-554 , 2020
Link:
https://doi.org/10.1111/..
?
15
Variant c.2158-2A>G in MANBA is an important and frequent c..:
Safka Brozkova, Dana
;
Varga, Lukas
;
Uhrova Meszarosova, Anna
...
Orphanet Journal of Rare Diseases. 15 (2020) 1 - p. , 2020
Link:
https://doi.org/10.1186/..
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